(1S,2R)-5-Benzyloxy-2-(1-methyl-3-phenyl-propylamino)-indan-1-ol; compound with (E)-but-2-enedioic acid

Base Information

Chemical Name:(1S,2R)-5-Benzyloxy-2-(1-methyl-3-phenyl-propylamino)-indan-1-ol; compound with (E)-but-2-enedioic acid
CAS No.:88628-01-7
Molecular Formula:C₄H₄O₄*2C₂₆H₂₉NO₂
Molecular Weight:891.117
Hs Code.:

Synonyms:(1S,2R)-5-Benzyloxy-2-(1-methyl-3-phenyl-propylamino)-indan-1-ol; compound with (E)-but-2-enedioic acid

Suppliers and Price of (1S,2R)-5-Benzyloxy-2-(1-methyl-3-phenyl-propylamino)-indan-1-ol; compound with (E)-but-2-enedioic acid

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of (1S,2R)-5-Benzyloxy-2-(1-methyl-3-phenyl-propylamino)-indan-1-ol; compound with (E)-but-2-enedioic acid

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (1S,2R)-5-Benzyloxy-2-(1-methyl-3-phenyl-propylamino)-indan-1-ol; compound with (E)-but-2-enedioic acid

There total 6 articles about (1S,2R)-5-Benzyloxy-2-(1-methyl-3-phenyl-propylamino)-indan-1-ol; compound with (E)-but-2-enedioic acid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 98.0%

: 2550-26-7
4-Phenyl-2-butanone

: 88628-64-2
(1S,2R)-2-Amino-5-benzyloxy-indan-1-ol; hydrochloride

: 110-17-8,26099-09-2
(2E)-but-2-enedioic acid

: 88628-01-7
(1S,2R)-5-Benzyloxy-2-(1-methyl-3-phenyl-propylamino)-indan-1-ol; compound with (E)-but-2-enedioic acid

Guidance literature:: With sodium cyanoborohydride; In methanol; diethyl ether; at 5 ℃;
DOI:10.1248/cpb.31.2329

Reference yield:

: 78326-88-2
5-benzyloxy-1-indanone

: 88628-01-7
(1S,2R)-5-Benzyloxy-2-(1-methyl-3-phenyl-propylamino)-indan-1-ol; compound with (E)-but-2-enedioic acid

Guidance literature:: Multi-step reaction with 3 steps

1: 70 percent / isoamilnitrite/conc. HCl / methanol / 0.5 h / 50 °C

2: 33 percent / 1.) LiAlH₄; 2.) HCl/EtOH / tetrahydrofuran / 7.5 h / Heating

3: 98 percent / 1.) NaBH₃CN / methanol; diethyl ether / 5 °C

With hydrogenchloride; lithium aluminium tetrahydride; ethanol; sodium cyanoborohydride; isopentyl nitrite; In tetrahydrofuran; methanol; diethyl ether;
DOI:10.1248/cpb.31.2329

Reference yield:

: 5111-70-6
5-methoxy-1-indanone

: 88628-01-7
(1S,2R)-5-Benzyloxy-2-(1-methyl-3-phenyl-propylamino)-indan-1-ol; compound with (E)-but-2-enedioic acid

Guidance literature:: Multi-step reaction with 5 steps

1: 84 percent / AlCl₃ / benzene / 1 h / Heating

2: 79 percent / K₂CO₃/KI / dimethylformamide / 2 h / 100 °C

3: 70 percent / isoamilnitrite/conc. HCl / methanol / 0.5 h / 50 °C

4: 33 percent / 1.) LiAlH₄; 2.) HCl/EtOH / tetrahydrofuran / 7.5 h / Heating

5: 98 percent / 1.) NaBH₃CN / methanol; diethyl ether / 5 °C

With hydrogenchloride; lithium aluminium tetrahydride; aluminium trichloride; ethanol; sodium cyanoborohydride; potassium carbonate; potassium iodide; isopentyl nitrite; In tetrahydrofuran; methanol; diethyl ether; N,N-dimethyl-formamide; benzene;
DOI:10.1248/cpb.31.2329