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18489-25-3

18489-25-3

Identification

Synonyms:5-(Phenylmethyl)-1H-tetrazole;

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Safety information and MSDS view more

  • Pictogram(s):HarmfulXn,IrritantXi

  • Hazard Codes:Xi,Xn

  • Signal Word:no data available

  • Hazard Statement:no data available

  • First-aid measures: General adviceConsult a physician. Show this safety data sheet to the doctor in attendance.If inhaled If breathed in, move person into fresh air. If not breathing, give artificial respiration. Consult a physician. In case of skin contact Wash off with soap and plenty of water. Consult a physician. In case of eye contact Rinse thoroughly with plenty of water for at least 15 minutes and consult a physician. If swallowed Never give anything by mouth to an unconscious person. Rinse mouth with water. Consult a physician.

  • Fire-fighting measures: Suitable extinguishing media Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide. Wear self-contained breathing apparatus for firefighting if necessary.

  • Accidental release measures: Use personal protective equipment. Avoid dust formation. Avoid breathing vapours, mist or gas. Ensure adequate ventilation. Evacuate personnel to safe areas. Avoid breathing dust. For personal protection see section 8. Prevent further leakage or spillage if safe to do so. Do not let product enter drains. Discharge into the environment must be avoided. Pick up and arrange disposal. Sweep up and shovel. Keep in suitable, closed containers for disposal.

  • Handling and storage: Avoid contact with skin and eyes. Avoid formation of dust and aerosols. Avoid exposure - obtain special instructions before use.Provide appropriate exhaust ventilation at places where dust is formed. For precautions see section 2.2. Store in cool place. Keep container tightly closed in a dry and well-ventilated place.

  • Exposure controls/personal protection:Occupational Exposure limit valuesBiological limit values Handle in accordance with good industrial hygiene and safety practice. Wash hands before breaks and at the end of workday. Eye/face protection Safety glasses with side-shields conforming to EN166. Use equipment for eye protection tested and approved under appropriate government standards such as NIOSH (US) or EN 166(EU). Skin protection Wear impervious clothing. The type of protective equipment must be selected according to the concentration and amount of the dangerous substance at the specific workplace. Handle with gloves. Gloves must be inspected prior to use. Use proper glove removal technique(without touching glove's outer surface) to avoid skin contact with this product. Dispose of contaminated gloves after use in accordance with applicable laws and good laboratory practices. Wash and dry hands. The selected protective gloves have to satisfy the specifications of EU Directive 89/686/EEC and the standard EN 374 derived from it. Respiratory protection Wear dust mask when handling large quantities. Thermal hazards

Supplier and reference price view more

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  • Manufacture/Brand:TRC
  • Product Description:5-Benzyl-1H-tetrazole
  • Packaging:500mg
  • Price:$ 60
  • Delivery:In stock
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  • Manufacture/Brand:TCI Chemical
  • Product Description:5-Benzyl-1H-tetrazole >98.0%(HPLC)(T)
  • Packaging:25g
  • Price:$ 125
  • Delivery:In stock
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  • Manufacture/Brand:Matrix Scientific
  • Product Description:5-Benzyl-1H-tetrazole
  • Packaging:1g
  • Price:$ 200
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  • Manufacture/Brand:Heterocyclics
  • Product Description:5-Benzyl-1H-tetrazole 98%
  • Packaging:25g
  • Price:$ 57
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  • Manufacture/Brand:Heterocyclics
  • Product Description:5-Benzyl-1H-tetrazole 98%
  • Packaging:100g
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  • Manufacture/Brand:Frontier Specialty Chemicals
  • Product Description:5-Benzyl-1H-tetrazole 99%
  • Packaging:5g
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  • Manufacture/Brand:Frontier Specialty Chemicals
  • Product Description:5-Benzyl-1H-tetrazole 99%
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  • Manufacture/Brand:Biosynth Carbosynth
  • Product Description:5-Benzyl-1H-tetrazole
  • Packaging:100 g
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  • Manufacture/Brand:Biosynth Carbosynth
  • Product Description:5-Benzyl-1H-tetrazole
  • Packaging:25 g
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  • Manufacture/Brand:Biosynth Carbosynth
  • Product Description:5-Benzyl-1H-tetrazole
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Relevant articles and documentsAll total 116 Articles be found

A rapid and green synthetic approach for hierarchically assembled porous ZnO nanoflakes with enhanced catalytic activity

Sinhamahapatra, Apurba,Giri, Arnab Kanti,Pal, Provas,Pahari, Sandip Kumar,Bajaj, Hari C.,Panda, Asit Baran

, p. 17227 - 17235 (2012)

Three dimensionally (3D) assembled hierarchical porous ZnO structures are of key importance for their applications in sensors, lithium-ion batteries, solar cells and in catalysis. Here, the controlled synthesis of 3D hierarchically porous ZnO architectures constructed of two dimensional (2D) nano-sheets through the calcination of a hydrozincite [Zn5(CO 3)2(OH)6] intermediate is presented. The intermediate 3D hierarchical hydrozincite has been synthesized by a novel organic surfactant and solvent free aqueous protocol at room temperature using an aqueous solution of ammonium carbonate and laboratory grade bulk ZnO in a short time (20-30 min). The amount of carbonate and the reaction temperature play a crucial role in the formation of the 3D hierarchical morphology and on the basis of the experimental results a probable reaction mechanism is proposed. On calcination, the synthesized 3D hierarchical hydrozincite resulted in ZnO with an almost identical morphology to the parental hydrozincite. On decomposition a porous structure having a surface area of 44 m2 g-1 is obtained. The synthesized hierarchical ZnO morphology exhibits an improved catalytic activity for the synthesis of 5-substituted-1H-tetrazoles with different nitriles and sodium azide than that of nanocrystalline ZnO and bulk ZnO, as well as other developed solid catalysts. The catalyst is easily recyclable without a significant loss in catalytic activity. The Royal Society of Chemistry 2012.

1-Disulfo-[2,2-bipyridine]-1,1-diium chloride ionic liquid as an efficient catalyst for the green synthesis of 5-substituted 1H-tetrazoles

Aali, Elaheh,Gholizadeh, Mostafa,Noroozi-Shad, Nazanin

, (2021/08/30)

A simple, green and efficient method has been developed for the synthesis of 5-substituted 1H-tetrazole derivatives through [2+3] cycloaddition reaction in good to excellent yields between various benzonitriles and sodium azide. For this purpose, 1-disulfo-[2,2-bipyridine]-1,1-diium chloride ([BiPy](HSO3)2Cl2) system as an ionic liquid catalyst have been extended for the construction of these valuable products. This procedure has significant advantages, including using ethylene glycol as a green solvent. The other advantages of this method are inexpensive and ease the preparation of the catalyst, mild reaction conditions, green reaction medium, easy workup, short reaction time, and simple experimental process.

Magnetic nitrogen-doped carbon derived from silk cocoon biomass: a promising and sustainable support for copper

Akbarzadeh, Parisa,Koukabi, Nadiya,Tahmasbi, Marzieh

, (2021/12/01)

In this study, a magnetic nitrogen-doped carbon-based copper (MNC-Cu) catalyst was fabricated so that natural silk cocoons undergo thermal processes and then activate by combining with Fe3O4 MNPs as a suitable substrate for placement copper metal. The efficiency of the generated catalyst in the synthesis of 5-substituted 1H-tetrazole derivatives was evaluated by the [3 + 2] cycloaddition reaction of aromatic aldehydes, azide ions, and hydroxylamines. FT-IR, FE-SEM, EDS, TEM, XRD, TGA, and VSM techniques have been adopted to identify and validate this heterogeneous catalyst. The observation from EDS, elemental mapping, XRD, and FT-IR analysis confirms the immobilization of Cu metals on the MNC surface and uniform distribution of species and then no aggregation occurs during functionalization. VSM results show the magnetic feature of fabricated catalyst, and based on the leaching test, the amount of catalyst leaching was negligible. Moreover, this reaction is a one-pot multicomponent reaction (MCRs) or more precisely a one-pot, three-component reaction, which is one of the advantages of this work. The fabricated catalyst shows high efficiency, good stability, and considerable reactivity in synthesizing 5-substituted 1H-tetrazole derivatives. So it can be seen that the fabricated magnetic catalyst is a useful and practical catalyst for synthesizing [3 + 2] cycloaddition reactions. Reusability and recyclability for five sequential runs without notable increase and reduction in activity are other advantages. In addition, the magnetic properties of this heterogeneous catalyst led to easy and quickly recovered and striking copper leaching. Graphical abstract: [Figure not available: see fulltext.]

Process route upstream and downstream products

Process route

5-benzyl-1-trityl-1H-tetrazole
147407-81-6

5-benzyl-1-trityl-1H-tetrazole

5-benzyl-1H-tetrazole
18489-25-3

5-benzyl-1H-tetrazole

Conditions
Conditions Yield
With naphthalene; lithium; In tetrahydrofuran; at -78 ℃; for 3h; Inert atmosphere;
82%
5-benzyl-1-trityl-1H-tetrazole; With methanol; indium; In tetrahydrofuran; at 78 ℃; for 25.5h;
With hydrogenchloride; In water; at 20 ℃;
80%
With methanol; zinc; In tetrahydrofuran; for 12h; Reflux;
75%
1,5-dibenzyl-1H-tetrazole
28386-91-6

1,5-dibenzyl-1H-tetrazole

5-benzyl-1H-tetrazole
18489-25-3

5-benzyl-1H-tetrazole

Conditions
Conditions Yield
With acetic acid; zinc; In tetrahydrofuran; at 20 ℃; Reagent/catalyst; Temperature; Cooling with ice;
87%
phenylacetonitrile
140-29-4

phenylacetonitrile

5-benzyl-1H-tetrazole
18489-25-3

5-benzyl-1H-tetrazole

Conditions
Conditions Yield
With sodium azide; In N,N-dimethyl-formamide; at 120 ℃; for 3h;
99%
With sodium azide; In dimethyl sulfoxide; at 110 ℃; for 1h; Green chemistry;
98%
With sodium azide; In water; at 100 ℃; for 0.0833333h; Reagent/catalyst;
98%
With sodium azide; at 120 ℃; for 0.0833333h; Reagent/catalyst;
98%
With sodium azide; 1,1'-disulfo-[2,2'-bipyridine]-1,1'-diium chloride; In ethylene glycol; at 80 ℃; Green chemistry;
98%
With sodium azide; acetic acid; In 1-methyl-pyrrolidin-2-one; water; at 220 ℃; for 0.166667h; under 12001.2 Torr; Microwave irradiation;
97%
With sodium azide; nickel(II) ferrite; ammonium acetate; In N,N-dimethyl-formamide; at 100 ℃; for 1h;
97%
With 1-methyl-pyrrolidin-2-one; chloro-trimethyl-silane; sodium azide; at 220 ℃; for 0.35h; Microwave irradiation;
96%
With 1-n-butyl-3-methylimidazolium azide; In neat (no solvent); at 110 ℃; for 0.75h; Green chemistry;
95%
With sodium azide; triethylamine hydrochloride; In toluene; at 110 ℃; for 16h; Inert atmosphere;
95%
With sodium azide; In N,N-dimethyl-formamide; at 90 ℃; for 4h; Solvent; Temperature; Time; chemoselective reaction; Inert atmosphere;
94%
With sodium azide; at 120 ℃; for 4.75h; Catalytic behavior; Green chemistry;
94%
With trimethylsilylazide; tetrabutyl ammonium fluoride; at 120 ℃; for 24h;
93%
phenylacetonitrile; With fipronilβ-cyclodextrin; In N,N-dimethyl-formamide; at 20 ℃; for 0.25h;
With sodium azide; ammonium chloride; In N,N-dimethyl-formamide; at 120 ℃; for 6h;
93%
With sodium azide; C12H10N4*8C8H5NO4(2-)*8Cu(2+)*2C3H7NO; at 110 ℃; for 0.166667h;
93%
With sodium azide; C12H16CuN4O4(2+)*2BF4(1-); In N,N-dimethyl-formamide; at 130 ℃; for 0.416667h; Microwave irradiation;
93%
With sodium azide; In N,N-dimethyl-formamide; at 50 ℃; for 2h; Green chemistry;
92%
With sodium azide; 5,10,15,20‐tetrakis‐(4‐sulfonatophenyl)‐porphyrin‐iron(III) chloride; In ethanol; water; at 60 ℃; for 73050h; Green chemistry;
92%
With sodium azide; at 120 ℃; for 4h;
91%
With sodium azide; In water; at 80 ℃; Catalytic behavior; Green chemistry;
91%
With sodium azide; triethylamine hydrochloride; In toluene; at 100 ℃; for 24h;
90%
With sodium azide; Acetate de N,N-dimethylamino-4 pyridinium; In neat (no solvent); at 100 ℃; for 3h;
90%
With sodium azide; at 120 ℃; for 0.333333h;
88%
With sodium azide; at 120 ℃; for 6.16667h; Catalytic behavior;
88%
With ziconium(IV) oxychloride octahydrate; sodium azide; In N,N-dimethyl-formamide; at 100 ℃; for 9h;
87%
With sodium azide; ammonium acetate; In N,N-dimethyl-formamide; at 120 ℃; for 8h;
87%
With sodium azide; ammonium cerium (IV) nitrate; In N,N-dimethyl-formamide; at 110 ℃; for 6h; Inert atmosphere; Green chemistry;
87%
With sodium azide; aluminum(III) hydrogen sulfate; In N,N-dimethyl-formamide; at 120 ℃; for 18h;
85%
With 1-n-butyl-3-methylimidazolium azide; In neat (no solvent); at 110 ℃; for 2h; Green chemistry;
85%
With sodium azide; (1,10-phenanthroline)bis(triphenylphosphine)copper(I) nitrate; In water; isopropyl alcohol; at 65 ℃; for 0.3h; Catalytic behavior; Inert atmosphere; Microwave irradiation; Green chemistry;
85%
phenylacetonitrile; With sodium azide; In water; at 20 ℃; for 0.5h;
With hydrogen bromide; In water; pH=1-2;
85%
phenylacetonitrile; With sodium azide; tris(pentafluorophenyl)borate; In N,N-dimethyl-formamide; at 120 ℃; for 12h;
With hydrogenchloride; In water; ethyl acetate; N,N-dimethyl-formamide; for 0.25h;
84%
With sodium azide; In N,N-dimethyl-formamide; at 100 ℃; for 6h; Reagent/catalyst; Temperature;
84%
With sodium azide; In N,N-dimethyl-formamide; at 100 ℃;
84%
With sodium azide; In water; at 100 ℃; for 8h; Catalytic behavior; Green chemistry;
84%
With sodium azide; L-proline; In N,N-dimethyl-formamide; at 110 ℃; Green chemistry;
84%
With sodium azide; acetic acid; In butan-1-ol; Heating;
83.5%
With sodium azide; In N,N-dimethyl-formamide; at 120 ℃; for 9h;
83%
With sodium azide; In N,N-dimethyl-formamide; at 110 ℃; for 8h;
83%
With sodium azide; In N,N-dimethyl-formamide; at 110 ℃; for 6h; Green chemistry;
83%
With sodium azide; zinc(II) chloride; In ethylene glycol; at 95 ℃; for 1h;
83%
With (CH3)2NH*HN3; In N,N-dimethyl-formamide; at 110 ℃; for 7h;
82%
With (CH3)2NH*HN3; In N,N-dimethyl-formamide; at 110 ℃; for 7h; Rate constant; Kinetics;
82%
With sodium azide; ammonium chloride; In N,N-dimethyl-formamide; at 120 ℃;
82%
phenylacetonitrile; With sodium azide; ammonium chloride; In N,N-dimethyl-formamide; for 12h; Reflux;
With hydrogenchloride; water; In N,N-dimethyl-formamide; pH=2;
81%
With sodium azide; In neat (no solvent); at 70 ℃; for 9h; Green chemistry;
81%
With sodium azide; zinc(II) chloride; In propan-1-ol; at 95 ℃; for 2h;
81%
With sodium azide; triethylamine hydrochloride; In nitrobenzene; at 100 ℃; for 2h; Microwave irradiation;
80%
With sodium azide; In N,N-dimethyl-formamide; at 120 ℃; for 14h;
80%
With indium(III) chloride; sodium azide; In N,N-dimethyl-formamide; for 0.116667h; Microwave irradiation;
80%
With sodium azide; copper(II) sulfate; In dimethyl sulfoxide; at 140 ℃; for 3h;
80%
With sodium azide; lead(II) chloride; In N,N-dimethyl-formamide; at 120 ℃; for 12h; Inert atmosphere;
80%
With sodium azide; In ethanol; at 80 ℃; for 10h;
80%
With sodium azide; In N,N-dimethyl-formamide; at 120 ℃; for 18h;
79%
With sodium azide; 1-ethyl-3-methylimidazolium hydrogensulfate; at 100 ℃; for 5h;
79%
With sodium azide; ammonium chloride; In N,N-dimethyl-formamide;
78%
With sodium azide; zinc(II) chloride; In water; at 95 ℃; for 6h; microwave irradiation;
78%
phenylacetonitrile; With sodium azide; tributyltin chloride; In o-xylene; for 3h; Reflux; Green chemistry;
With sodium hydroxide; In o-xylene; water; at 20 ℃; for 1h; Green chemistry;
With hydrogenchloride; In water; at 5 - 10 ℃; pH=2; Green chemistry;
78%
With sodium azide; at 120 ℃; for 24h; Green chemistry;
77%
With trimethylsilylazide; In acetone; at 200 ℃; for 0.125h; Flow reactor;
77%
phenylacetonitrile; With sodium azide; In water; at 100 ℃; for 1.5h; Green chemistry;
With hydrogenchloride; In water; at 20 ℃; for 0.00833333h; chemoselective reaction; Catalytic behavior; Green chemistry;
77%
phenylacetonitrile; With sodium azide; In N,N-dimethyl-formamide; at 120 ℃; for 36h;
With hydrogenchloride; In water; ethyl acetate; for 0.0833333h;
76%
With sodium azide; In dimethyl sulfoxide; at 130 ℃; for 5h; Green chemistry;
75%
With sodium azide; In dimethyl sulfoxide; at 120 ℃; for 5h;
75%
With sodium azide; In N,N-dimethyl-formamide; for 3.3h; Sonication;
75%
With sodium azide; In dimethyl sulfoxide; at 85 ℃; for 12h;
74%
With sodium azide; at 120 ℃; for 24h;
74%
With sodium azide; glycerol; at 110 ℃; for 3h;
73%
With hydrogenchloride; sodium azide; water; triethylamine hydrochloride; In toluene; at 95 - 99 ℃; for 1h;
71%
With antimony(III) trioxide; sodium azide; In N,N-dimethyl-formamide; at 130 ℃; for 20h;
71%
With iron(III) oxide; sodium azide; In N,N-dimethyl-formamide; at 120 ℃; for 36h;
71%
With sodium azide; In N,N-dimethyl-formamide; at 120 ℃; for 24h;
71.4%
With phosphomolybdic acid; sodium azide; In N,N-dimethyl-formamide; at 80 ℃; for 4.5h;
71%
With sodium azide; In N,N-dimethyl-formamide; at 120 ℃; for 30h;
71%
With ammonium chloride; In N-methyl-acetamide;
70%
70.7%
With sodium azide; In N,N-dimethyl-formamide; at 110 ℃;
70%
With sodium azide; acetic acid; urea; In water; N,N-dimethyl-formamide; at 60 - 110 ℃; for 9h;
70%
With sodium azide; at 100 ℃; for 14h;
70%
With sodium azide; at 130 ℃; for 0.283333h; Microwave irradiation; Neat (no solvent);
69%
With sodium azide; zinc hydroxide carbonate; In N,N-dimethyl-formamide; at 125 ℃; for 20h;
68%
With sodium azide; zinc(II) oxide; In N,N-dimethyl-formamide; at 125 ℃; for 14h; Green chemistry;
68%
With sodium azide; In N,N-dimethyl-formamide; at 120 ℃; for 24h;
67%
With copper(I) oxide; methanol; trimethylsilylazide; In N,N-dimethyl-formamide; at 80 ℃; for 24h;
66%
With sodium azide; triethylamine hydrochloride; In toluene; at 110 ℃; for 17h;
63%
With sodium azide; triethylamine hydrochloride; In toluene; at 110 ℃; for 17h;
63%
With sodium azide; triethylamine hydrochloride; In toluene; at 110 ℃; for 17h;
63%
With trimethylsilylazide; at 140 ℃; for 4h; Reagent/catalyst; Temperature; Sealed tube;
63%
phenylacetonitrile; With sodium azide; cadmium(II) chloride; In N,N-dimethyl-formamide; at 80 ℃; for 12h;
With hydrogenchloride; water; In ethyl acetate;
62%
With sodium azide; copper(II) nitrate trihydrate; In N,N-dimethyl-formamide; at 120 ℃; for 16h;
62%
With hydrogenchloride; sodium azide; triethylamine; In toluene; at 110 ℃;
56%
With sodium azide; ammonium chloride; In N,N-dimethyl-formamide; for 7h; Heating;
50%
With sodium azide; cerium(III) chloride heptahydrate; In water; isopropyl alcohol; at 160 ℃; for 4h; Microwave irradiation;
48%
With sodium azide; In N,N-dimethyl-formamide; at 110 ℃; for 10h;
48%
With sodium azide; 1H,4H-piperazine-N,N'-diium hydrogensulfate; at 100 ℃; for 3h;
35%
With sodium azide; triethylamine hydrochloride; In toluene; at 110 ℃;
25%
With ammonium azide; N,N-dimethyl-formamide; lithium chloride; at 125 ℃;
With tris-(2-chloro-ethyl)-amine; benzene; at 150 ℃;
With sodium azide; zinc dibromide; In 1-methyl-pyrrolidin-2-one; water; at 190 ℃; for 0.333333h; optical yield given as %ee;
With sodium azide; iodine; In tetrahydrofuran; water; at 100 ℃; for 12h;
Phenylacetaldehyde oxime
7028-48-0

Phenylacetaldehyde oxime

5-benzyl-1H-tetrazole
18489-25-3

5-benzyl-1H-tetrazole

Conditions
Conditions Yield
With diphenyl phosphoryl azide; 1,8-diazabicyclo[5.4.0]undec-7-ene; In 5,5-dimethyl-1,3-cyclohexadiene; for 16h; Solvent; Reflux; Green chemistry;
86%
With sodium azide; hydroxylamine hydrochloride; In water; at 70 ℃; for 5.66667h; Green chemistry;
75%
With diphenyl phosphoryl azide; 1,8-diazabicyclo[5.4.0]undec-7-ene; In toluene; for 48h; Reflux;
71%
(E)-2-phenylacetaldehyde oxime
20268-21-7

(E)-2-phenylacetaldehyde oxime

5-benzyl-1H-tetrazole
18489-25-3

5-benzyl-1H-tetrazole

Conditions
Conditions Yield
With sodium azide; copper(II) ferrite; In N,N-dimethyl-formamide; at 120 ℃; for 12h; Sealed tube;
72%
5-(2',6'-dichlorobenzyl)-1H-tetrazole
51449-78-6

5-(2',6'-dichlorobenzyl)-1H-tetrazole

5-benzyl-1H-tetrazole
18489-25-3

5-benzyl-1H-tetrazole

Conditions
Conditions Yield
palladium on activated carbon; In methanol;
potassium cyanide

potassium cyanide

benzyl boronic acid
4463-42-7

benzyl boronic acid

5-benzyl-1H-tetrazole
18489-25-3

5-benzyl-1H-tetrazole

Conditions
Conditions Yield
With sodium azide; potassium carbonate; In ethanol; water; for 6h; Catalytic behavior; Reflux; Inert atmosphere; Green chemistry;
84%
C<sub>20</sub>H<sub>34</sub>N<sub>4</sub>Sn
34833-34-6

C20H34N4Sn

5-benzyl-1H-tetrazole
18489-25-3

5-benzyl-1H-tetrazole

Conditions
Conditions Yield
C20H34N4Sn; With sodium hydroxide; In o-xylene; water; at 20 ℃; for 1h;
With hydrogenchloride; In water; at 5 - 10 ℃; pH=2;
phenyl(1H-tetrazol-5-yl)methanone
14506-41-3

phenyl(1H-tetrazol-5-yl)methanone

5-benzyl-1H-tetrazole
18489-25-3

5-benzyl-1H-tetrazole

Conditions
Conditions Yield
With potassium hydroxide; hydrazine hydrate; diethylene glycol;
(±)-phenyl(1H-tetrazol-5-yl)methanol
40060-76-2

(±)-phenyl(1H-tetrazol-5-yl)methanol

5-benzyl-1H-tetrazole
18489-25-3

5-benzyl-1H-tetrazole

Conditions
Conditions Yield
Multi-step reaction with 2 steps
1: Na2Cr2O7; aqueous H2SO4
2: KOH; diethylene glycol; N2H4+H2O
With potassium hydroxide; sodium dichromate; sulfuric acid; hydrazine hydrate; diethylene glycol;

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