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699-12-7 Usage

Chemical Properties

clear colorless to yellow liquid

Uses

2-(Phenylthio)ethanol has been used:in the synthesis of indole, benzofuran and benzothiophenefor temporary masking of the thymine residue during the synthesis of sugar modified thymidine derivativesin the preparation of 4-[2-(phenylthio)ethoxy]phthalonitrile

Synthesis Reference(s)

Synthesis, p. 641, 1975 DOI: 10.1055/s-1975-23865

Check Digit Verification of cas no

The CAS Registry Mumber 699-12-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,9 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 699-12:
(5*6)+(4*9)+(3*9)+(2*1)+(1*2)=97
97 % 10 = 7
So 699-12-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H10OS/c9-6-7-10-8-4-2-1-3-5-8/h1-5,9H,6-7H2

699-12-7 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
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  • Detail
  • Alfa Aesar

  • (A10861)  2-(Phenylthio)ethanol, 99%   

  • 699-12-7

  • 10g

  • 307.0CNY

  • Detail
  • Alfa Aesar

  • (A10861)  2-(Phenylthio)ethanol, 99%   

  • 699-12-7

  • 50g

  • 904.0CNY

  • Detail
  • Aldrich

  • (232777)  2-(Phenylthio)ethanol  99%

  • 699-12-7

  • 232777-50G

  • 666.90CNY

  • Detail

699-12-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(Phenylthio)ethanol

1.2 Other means of identification

Product number -
Other names 2-phenylsulfanylethanol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:699-12-7 SDS

699-12-7Synthetic route

O-trimethylsilyl-S-phenylethylene monothioglycol
16654-71-0

O-trimethylsilyl-S-phenylethylene monothioglycol

2-(phenylthio)ethanol
699-12-7

2-(phenylthio)ethanol

Conditions
ConditionsYield
With water; 1,1,1,3,3,3-hexamethyl-disilazane In dichloromethane at 20℃; for 0.616667h;96%
2-(phenylsulfinyl)ethanol
123299-91-2, 22063-21-4

2-(phenylsulfinyl)ethanol

2-(phenylthio)ethanol
699-12-7

2-(phenylthio)ethanol

Conditions
ConditionsYield
With 1,3,5-trichloro-2,4,6-triazine; potassium iodide In acetonitrile at 20℃; for 0.133333h; chemoselective reaction;95%
With titanium(IV) iodide In acetonitrile at 0℃; for 0.166667h; Reduction;87%
With sodium iodide at 20℃; for 4h; Green chemistry;87%
iodobenzene
591-50-4

iodobenzene

2-hydroxyethanethiol
60-24-2

2-hydroxyethanethiol

2-(phenylthio)ethanol
699-12-7

2-(phenylthio)ethanol

Conditions
ConditionsYield
With copper(l) iodide; potassium phosphate tribasic trihydrate at 110℃; for 12h;95%
With potassium phosphate In neat (no solvent) at 70℃; for 9h;70%
With potassium hydroxide In dimethyl sulfoxide at 110℃; for 8h; Inert atmosphere;67%
2-(phenylthio)acetaldehyde
66303-55-7

2-(phenylthio)acetaldehyde

2-(phenylthio)ethanol
699-12-7

2-(phenylthio)ethanol

Conditions
ConditionsYield
With lithium aluminium tetrahydride In tetrahydrofuran at -78℃;95%
C14H13NO3S2

C14H13NO3S2

2-(phenylthio)ethanol
699-12-7

2-(phenylthio)ethanol

Conditions
ConditionsYield
With triethylamine In dichloromethane for 14h; Irradiation;93%
C14H12N2O5S2

C14H12N2O5S2

2-(phenylthio)ethanol
699-12-7

2-(phenylthio)ethanol

Conditions
ConditionsYield
With triethylamine In dichloromethane for 5.5h; Irradiation;93%
chlorobenzene
108-90-7

chlorobenzene

2-hydroxyethanethiol
60-24-2

2-hydroxyethanethiol

2-(phenylthio)ethanol
699-12-7

2-(phenylthio)ethanol

Conditions
ConditionsYield
With potassium phosphate In neat (no solvent) at 70℃; for 10h;40%
2-Chloroethyl phenyl sulfide
5535-49-9

2-Chloroethyl phenyl sulfide

water
7732-18-5

water

2-(phenylthio)ethanol
699-12-7

2-(phenylthio)ethanol

Conditions
ConditionsYield
With HKUST-1 metal organic framework In tetrachloromethane at 20℃; Kinetics;38%
oxirane
75-21-8

oxirane

thiophenol
108-98-5

thiophenol

2-(phenylthio)ethanol
699-12-7

2-(phenylthio)ethanol

Conditions
ConditionsYield
With pyrographite
With sodium hydroxide
thiophenol
108-98-5

thiophenol

2-chloro-ethanol
107-07-3

2-chloro-ethanol

2-(phenylthio)ethanol
699-12-7

2-(phenylthio)ethanol

Conditions
ConditionsYield
With sodium ethanolate
With sodium hydroxide
With sodium hydroxide
2-fluoroethanol
371-62-0

2-fluoroethanol

thiophenol
108-98-5

thiophenol

2-(phenylthio)ethanol
699-12-7

2-(phenylthio)ethanol

Conditions
ConditionsYield
With sodium hydroxide
sodium thiophenolate
930-69-8

sodium thiophenolate

2-chloro-ethanol
107-07-3

2-chloro-ethanol

2-(phenylthio)ethanol
699-12-7

2-(phenylthio)ethanol

oxirane
75-21-8

oxirane

Tetrathiophosphoric acid diphenyl ester; compound with triethyl-amine
18863-43-9

Tetrathiophosphoric acid diphenyl ester; compound with triethyl-amine

A

2-(phenylthio)ethanol
699-12-7

2-(phenylthio)ethanol

B

2-Phenylsulfanyl-[1,3,2]oxathiaphospholane 2-sulfide

2-Phenylsulfanyl-[1,3,2]oxathiaphospholane 2-sulfide

Conditions
ConditionsYield
With boron trifluoride diethyl etherate In chloroform at -30 - 20℃; for 12h;
formaldehyd
50-00-0

formaldehyd

methyl-phenyl-thioether
100-68-5

methyl-phenyl-thioether

2-(phenylthio)ethanol
699-12-7

2-(phenylthio)ethanol

Conditions
ConditionsYield
With n-butyllithium; N,N,N,N,-tetramethylethylenediamine Multistep reaction;
1-bromo-2-phenylthioethane
4837-01-8

1-bromo-2-phenylthioethane

2-(phenylthio)ethanol
699-12-7

2-(phenylthio)ethanol

Conditions
ConditionsYield
With water Kinetics; Mechanism;
ethylene glycol
107-21-1

ethylene glycol

thiophenol
108-98-5

thiophenol

2-(phenylthio)ethanol
699-12-7

2-(phenylthio)ethanol

Conditions
ConditionsYield
With potassium hydroxide In N,N-dimethyl acetamide
Naphthalene-2-sulfonic acid 2-phenylsulfanyl-ethyl ester

Naphthalene-2-sulfonic acid 2-phenylsulfanyl-ethyl ester

A

2-(phenylthio)ethanol
699-12-7

2-(phenylthio)ethanol

B

N-(2-hydroxyethyl)-naphthalene-2-sulfonamide
72005-23-3

N-(2-hydroxyethyl)-naphthalene-2-sulfonamide

Conditions
ConditionsYield
With potassium hydroxide In dimethyl sulfoxide at 25℃; Rate constant; var. solvents;
2-(phenylthio)ethyl brosylate
114396-25-7

2-(phenylthio)ethyl brosylate

methylamine
74-89-5

methylamine

A

2-(phenylthio)ethanol
699-12-7

2-(phenylthio)ethanol

B

4-bromo-N-(2-hydroxy-ethyl)-benzenesulfonamide
59724-43-5

4-bromo-N-(2-hydroxy-ethyl)-benzenesulfonamide

Conditions
ConditionsYield
With potassium hydroxide In dimethyl sulfoxide at 25℃; Rate constant; var. solvents;
2-(phenylthio)ethanol
699-12-7

2-(phenylthio)ethanol

2-(phenylsulfonyl)ethanol
20611-21-6

2-(phenylsulfonyl)ethanol

Conditions
ConditionsYield
With dihydrogen peroxide; phosphotungstate-non-cross-linked amphiphilic polymer compl at 50℃; for 4h;100%
With phosphotungstic acid; poly(acrylamide) based ammonium salt; dihydrogen peroxide at 50℃; for 4h;100%
With dihydrogen peroxide; titanium(IV) oxide In acetonitrile at 20℃; for 1.5h; chemoselective reaction;100%
2-(phenylthio)ethanol
699-12-7

2-(phenylthio)ethanol

2-(phenylsulfinyl)ethanol
123299-91-2, 22063-21-4

2-(phenylsulfinyl)ethanol

Conditions
ConditionsYield
With iron(III) chloride; periodic acid In acetonitrile at 0 - 25℃; for 0.416667h;100%
With aluminum(III) nitrate nonahydrate; sulfuric acid; silica gel; silica gel; sodium bromide In dichloromethane; water at 20℃; for 3.5h; chemoselective reaction;99%
With water; ammonium bromide In dichloromethane at 20℃; for 8h; chemoselective reaction;99%
2-(phenylthio)ethanol
699-12-7

2-(phenylthio)ethanol

2-(phenylthio)acetaldehyde
66303-55-7

2-(phenylthio)acetaldehyde

Conditions
ConditionsYield
With 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione In ethyl acetate for 8h; Heating;100%
With 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione In dimethyl sulfoxide at 20℃; for 4h;90%
With 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione In dimethyl sulfoxide at 10 - 30℃; for 8h;42%
2-(phenylthio)ethanol
699-12-7

2-(phenylthio)ethanol

tert-butyldimethylsilane
29681-57-0

tert-butyldimethylsilane

1-(t-BuMe2Si)-2-(t-BuMe2Si-S)ethyl ether
82112-28-5

1-(t-BuMe2Si)-2-(t-BuMe2Si-S)ethyl ether

Conditions
ConditionsYield
With palladium dichloride In N,N-dimethyl acetamide at 24.85℃; for 3h;100%
2-(phenylthio)ethanol
699-12-7

2-(phenylthio)ethanol

1-bromo-2-phenylthioethane
4837-01-8

1-bromo-2-phenylthioethane

Conditions
ConditionsYield
With carbon tetrabromide; Cu(tmp)(BINAP)BF4; sodium bromide In N,N-dimethyl-formamide for 24h; Appel Halogenation; UV-irradiation; Inert atmosphere;99%
With sulfurous dibromide; N,N-dimethyl-formamide In cyclohexane at 20℃; for 3h; Bromination;98%
With phosphorus tribromide at 20℃; for 0.5h;98%
tert.-butylhydroperoxide
75-91-2

tert.-butylhydroperoxide

bis{rhodium[3,3'-(1,3-phenylene)bis(2,2-dimethylpropanoic acid)]}

bis{rhodium[3,3'-(1,3-phenylene)bis(2,2-dimethylpropanoic acid)]}

2-(phenylthio)ethanol
699-12-7

2-(phenylthio)ethanol

Rh2(α,α,α′,α′-tetramethyl-1,3-benzenedipropanoate)2-bis-2-(phenylsulfinyl)ethanol

Rh2(α,α,α′,α′-tetramethyl-1,3-benzenedipropanoate)2-bis-2-(phenylsulfinyl)ethanol

Conditions
ConditionsYield
In dichloromethane at 20℃; for 9h;99%
2-(phenylthio)ethanol
699-12-7

2-(phenylthio)ethanol

2-Chloroethyl phenyl sulfide
5535-49-9

2-Chloroethyl phenyl sulfide

Conditions
ConditionsYield
With 1,3,5-trichloro-2,4,6-triazine; N,N-dimethyl-formamide In dichloromethane at 25℃; for 48h;98%
With thionyl chloride96%
With hydrogenchloride; tetrafluoroboric acid In hydrogenchloride72.4%
2-(phenylthio)ethanol
699-12-7

2-(phenylthio)ethanol

C34H37NO5Si
144127-38-8

C34H37NO5Si

C36H41NO5SSi
144127-41-3

C36H41NO5SSi

Conditions
ConditionsYield
With sodium hydride In tetrahydrofuran at 0℃; for 0.0833333h;98%
2-(phenylthio)ethanol
699-12-7

2-(phenylthio)ethanol

Conditions
ConditionsYield
With sodium hydride In tetrahydrofuran at 0℃; for 0.0833333h;96%
With 18-crown-6 ether; caesium carbonate In acetonitrile at 25℃; for 12h;
2-(phenylthio)ethanol
699-12-7

2-(phenylthio)ethanol

A

2-(phenylsulfinyl)ethanol
123299-91-2, 22063-21-4

2-(phenylsulfinyl)ethanol

B

2-(phenylsulfonyl)ethanol
20611-21-6

2-(phenylsulfonyl)ethanol

Conditions
ConditionsYield
With dihydrogen peroxide In water at 30℃; for 1h;A 94%
B 6%
With dihydrogen peroxide at 50℃; for 4h;A 80%
B 13%
With (Bu4N)2[{MoO(O2)2}2(μ-O)]; dihydrogen peroxide In acetonitrile for 2h; Time;A 66%
B 30%
(2-hydroxyethyl)(methyl)amine
109-83-1

(2-hydroxyethyl)(methyl)amine

bis(trichloromethyl) carbonate
32315-10-9

bis(trichloromethyl) carbonate

2-(phenylthio)ethanol
699-12-7

2-(phenylthio)ethanol

C12H17NO3S

C12H17NO3S

Conditions
ConditionsYield
Stage #1: bis(trichloromethyl) carbonate; 2-(phenylthio)ethanol With pyridine In tetrahydrofuran at 20℃; for 0.75h; Cooling with ice;
Stage #2: With pyridine; 1-hydroxy-pyrrolidine-2,5-dione In tetrahydrofuran at 20℃; for 0.5h;
Stage #3: (2-hydroxyethyl)(methyl)amine In tetrahydrofuran at 20℃; for 2h; Cooling with ice;
93%
2-(phenylthio)ethanol
699-12-7

2-(phenylthio)ethanol

C45H39NO4Si
144127-84-4

C45H39NO4Si

C47H43NO4SSi
144127-85-5

C47H43NO4SSi

Conditions
ConditionsYield
With sodium hydride In tetrahydrofuran at 25℃; for 0.166667h;92%
2-(phenylthio)ethanol
699-12-7

2-(phenylthio)ethanol

D-glucal triacetate
2873-29-2

D-glucal triacetate

Acetic acid (2R,3S)-2-acetoxymethyl-6-(2-phenylsulfanyl-ethoxy)-3,6-dihydro-2H-pyran-3-yl ester
121237-63-6, 121252-52-6

Acetic acid (2R,3S)-2-acetoxymethyl-6-(2-phenylsulfanyl-ethoxy)-3,6-dihydro-2H-pyran-3-yl ester

Conditions
ConditionsYield
With boron trifluoride diethyl etherate In benzene for 0.133333h; Ambient temperature;92%
3,4-dihydro-2H-pyran
110-87-2

3,4-dihydro-2H-pyran

2-(phenylthio)ethanol
699-12-7

2-(phenylthio)ethanol

2-(2-phenylsulfanyl-ethoxy)-tetrahydro-pyran

2-(2-phenylsulfanyl-ethoxy)-tetrahydro-pyran

Conditions
ConditionsYield
With ruthenium(III) acetate at 20℃; for 24h;92%
2-(phenylthio)ethanol
699-12-7

2-(phenylthio)ethanol

C29H25NO4S
144127-43-5

C29H25NO4S

Conditions
ConditionsYield
With 18-crown-6 ether; caesium carbonate In acetonitrile at 25℃; for 45h;91%
2-(phenylthio)ethanol
699-12-7

2-(phenylthio)ethanol

trifluoroacetic anhydride
407-25-0

trifluoroacetic anhydride

2-(phenylthio)ethyl trifluoroacetate
52060-27-2

2-(phenylthio)ethyl trifluoroacetate

Conditions
ConditionsYield
With pyridine In dichloromethane at 0℃; for 2h;91%
2-amino-benzthiazole
136-95-8

2-amino-benzthiazole

2-(phenylthio)ethanol
699-12-7

2-(phenylthio)ethanol

N-(2-(phenylthio)ethyl)benzo[d]thiazol-2-amine
1353280-20-2

N-(2-(phenylthio)ethyl)benzo[d]thiazol-2-amine

Conditions
ConditionsYield
With bis[dichloro(pentamethylcyclopentadienyl)iridium(III)]; sodium hydroxide at 150℃; for 12h; Inert atmosphere; regioselective reaction;91%
2-(phenylthio)ethanol
699-12-7

2-(phenylthio)ethanol

C29H25NO4S
144127-39-9

C29H25NO4S

Conditions
ConditionsYield
With sodium hydride In tetrahydrofuran at 0℃; for 0.0833333h;90%
With 18-crown-6 ether; caesium carbonate In acetonitrile at 25℃; for 12h;
2-(phenylthio)ethanol
699-12-7

2-(phenylthio)ethanol

5'-O-tert-butyldimethylsilyl-3'-O-(4,4'-dimethoxytriphenylmethyl)thymidine
164267-52-1

5'-O-tert-butyldimethylsilyl-3'-O-(4,4'-dimethoxytriphenylmethyl)thymidine

1-[4-[bis-(4-methoxy-phenyl)-phenyl-methoxy]-5-(tert-butyl-dimethyl-silanyloxymethyl)-tetrahydro-furan-2-yl]-5-methyl-3-(2-phenylsulfanyl-ethyl)-1H-pyrimidine-2,4-dione
903570-37-6

1-[4-[bis-(4-methoxy-phenyl)-phenyl-methoxy]-5-(tert-butyl-dimethyl-silanyloxymethyl)-tetrahydro-furan-2-yl]-5-methyl-3-(2-phenylsulfanyl-ethyl)-1H-pyrimidine-2,4-dione

Conditions
ConditionsYield
With tributylphosphine; 1,1'-azodicarbonyl-dipiperidine In benzene at 20℃; for 18h; Mitsunobu reaction;90%
1-(4-nitrophenyl)-5-tetrazolone
75430-97-6

1-(4-nitrophenyl)-5-tetrazolone

2-(phenylthio)ethanol
699-12-7

2-(phenylthio)ethanol

diethylazodicarboxylate
1972-28-7

diethylazodicarboxylate

1-(4-Nitrophenyl)-4-(2-phenylsulfanylethyl)-1,4-dihydrotetrazol-5-one

1-(4-Nitrophenyl)-4-(2-phenylsulfanylethyl)-1,4-dihydrotetrazol-5-one

Conditions
ConditionsYield
With triphenylphosphine In tetrahydrofuran90%
1-(4-nitrophenyl)-5-tetrazolone
75430-97-6

1-(4-nitrophenyl)-5-tetrazolone

2-(phenylthio)ethanol
699-12-7

2-(phenylthio)ethanol

1-(4-Nitrophenyl)-4-(2-phenylsulfanylethyl)-1,4-dihydrotetrazol-5-one

1-(4-Nitrophenyl)-4-(2-phenylsulfanylethyl)-1,4-dihydrotetrazol-5-one

Conditions
ConditionsYield
With triphenylphosphine; diethylazodicarboxylate In tetrahydrofuran for 12h;90%
2-(phenylthio)ethanol
699-12-7

2-(phenylthio)ethanol

methacrylic acid methyl ester
80-62-6

methacrylic acid methyl ester

2-phenylthioethyl methacrylate
95175-52-3

2-phenylthioethyl methacrylate

Conditions
ConditionsYield
With titanium(IV) isopropylate; 2,4-dimethyl-6-tert-butylphenol; pyrographite In cyclohexane at 90 - 92℃;90%
2-(phenylthio)ethanol
699-12-7

2-(phenylthio)ethanol

1,1,1,3,3,3-hexamethyl-disilazane
999-97-3

1,1,1,3,3,3-hexamethyl-disilazane

O-trimethylsilyl-S-phenylethylene monothioglycol
16654-71-0

O-trimethylsilyl-S-phenylethylene monothioglycol

Conditions
ConditionsYield
With asymmetric salen type di-Schiff base-based zinc complex supported on Fe3O4 nanoparticles at 20℃; for 0.416667h;89%
With cross-linked poly((30percent)4-vinylpyridine/(70percent)styrene) copolymer-supported bismuth(III) triflate In dichloromethane at 20℃; for 0.166667h;86%
With chloro-trimethyl-silane
2-(phenylthio)ethanol
699-12-7

2-(phenylthio)ethanol

thiophenol
108-98-5

thiophenol

1,2-bis(phenylthio)ethane
622-20-8

1,2-bis(phenylthio)ethane

Conditions
ConditionsYield
With toluene-4-sulfonic acid In toluene for 3h; Heating;89%

699-12-7Relevant articles and documents

A novel CuO NPs/AgZSM-5 zeolite composite adsorbent: Synthesis, identification and its application for the removal of sulfur mustard agent simulant

Sadeghi, Meysam,Yekta, Sina,Mirzaei, Daryoush

, p. 995 - 1005 (2018)

In this investigation, the parent NaZSM-5 zeolite has been successfully fabricated by the hydrothermal route and then to enhance the catalytic performance of this zeolite, silver ions (Ag+) and copper oxide nanoparticles (CuO NPs) were loaded in its structure through the ion exchange and impregnation methods to attain the novel CuO NPs/AgZSM-5 zeolite composite adsorbent. The parent and modified samples were comprehensively analyzed and identified by using the FESEM-EDX, TEM, XRD, and FTIR techniques. This is the first time that the CuO NPs/AgZSM-5 (containing 3.4 wt% Ag and 12.6 wt% CuO) has been utilized for the removal (adsorption and degradation) of 2-chloroethyl phenyl sulfide (2-CEPS) as a toxic sulfur mustard agent simulate, and its applicability was proved according to the GC-FID, GC-MS, and FTIR results. Moreover, the consequences of several experimental factors such as contact time, initial concentration, adsorbent dose, and adsorbent type on the removal efficiency of 2-CEPS were also surveyed. The GC-FID analysis data confirmed that the maximum removal yield of 2-CEPS was 100%. Besides, the parameters of contact time (120 min), initial concentration (25 mg/L), and adsorbent dose (0.3 g) were perused and optimized for the subsequent reaction. The reaction kinetic status was also studied employing first order model. The quantities of the half-life (t1/2) and rate constant (k) were indicated as 26.25 min and 0.0264 min?1, respectively. The product obtained from the degradation and hydrolysis reaction between the 2-CEPS and CuO NPs/AgZSM-5 was 2-hydroxy ethyl phenyl sulfide (2-HEPS) which is substantially less toxic than original pesticide.

An asymmetric Salamo-based Zn complex supported on Fe3O4MNPs: a novel heterogeneous nanocatalyst for the silyl protection and deprotection of alcohols under mild conditions

Yao, Hongyan,Wang, Yongsheng,Razi, Maryam Kargar

, p. 12614 - 12625 (2021/04/14)

In this study, a magnetic asymmetric Salamo-based Zn complex (H2L = salen type di-Schiff bases)-supported on the surface of modified Fe3O4(Fe3O4@H2L-Zn) as a new catalyst was designed and characterizedvianumerous analytical techniques such as FT-IR spectroscopy, XRD, EDS, ICP-AES, SEM, TEM, TGA and VSM. An efficient and sustainable synthetic protocol has been presented for the synthesis of silyl ether substructuresviathe silyl protection of alcohols under mild conditions. The synthetic protocol involves a two-component solvent-free reaction between various hydroxyl-bearing substrates and hexamethyldisilazane (HMDS) as an inexpensive silylating agent using Fe3O4@H2L-Zn MNPs as a magnetically separable, recyclable and reusable heterogeneous catalyst. Fe3O4@H2L-Zn MNPs were also applied for the removal of silyl protecting groups from hydroxyl functions using water in CH2Cl2under green conditions. The catalyst demonstrated good to excellent catalytic yield efficiency for both the reactions compared to the commercial metal-based catalysts under green conditions for a wide range of substrates.

C-S cross-coupling reaction using novel and green synthesized CuO nanoparticles assisted by Euphorbia maculata extract

Alinezhad, Heshmatollah,Pakzad, Khatereh

, (2019/08/20)

In the present study, biosynthesis of CuO nanoparticles using a rapid, eco-friendly, cost-effective and efficient method has been reported employing aqueous Euphorbia maculata extract as mild, renewable and non-toxic reducing and capping agents without adding any surfactants. The biogenic and green method has some benefits compared to conventional physical and chemical methods. It is simple, cheap and environmentally friendly. The biosynthesized CuO NP displayed a color change pattern (from sky blue to black) on preparation and presented its respective broad peak at 365?nm, which was analyzed by UV–Vis spectroscopy. Using the FT-IR analysis, biomolecules in E. maculata extract which are responsible for bioreduction activity and synthesize of CuO NP, were identified. The XRD, EDX and FESEM results confirmed the successful synthesis of CuO nanoparticles of 18?nm sizes, with spherical and sponge crystal structure. The catalytic activity of biosynthesized CuO NPs was studied in C-S cross-coupling reaction. This method has the advantages of high yields, easy work-up, and simple reusability. The recovered CuO NP can be reused four times without any considerable loss of its catalytic activity.

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