(1R,2R)-1--1-phenylpropan-2-ol

Base Information

Chemical Name:(1R,2R)-1--1-phenylpropan-2-ol
CAS No.:255060-81-2
Molecular Formula:C₁₄H₂₁NO₃
Molecular Weight:251.326
Hs Code.:

(1R,2R)-1-<n-(tert-butoxycarbonyl)amino>-1-phenylpropan-2-ol

Synonyms:(1R,2R)-1--1-phenylpropan-2-ol

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

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Chemical Property of (1R,2R)-1--1-phenylpropan-2-ol

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Technology Process of (1R,2R)-1--1-phenylpropan-2-ol

There total 11 articles about (1R,2R)-1--1-phenylpropan-2-ol 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: 82.0%

: 310450-38-5
(1R,2S,R_S)-N-(tert-butoxycarbonyl)-1-amino-1-phenyl-3-(p-tolylsulfinyl)-2-propanol

: 255060-81-2
(1R,2R)-1--1-phenylpropan-2-ol

Guidance literature:: With nickel; In methanol; at 20 ℃; for 1h;
DOI:10.1016/S0957-4166(00)00264-0

Reference yield:

: 255060-80-1
(1R,2R)-1-[N-(tert-butoxycarbonyl)amino]-1-phenyl-2-propyl 4-nitrobenzoate

: 255060-81-2
(1R,2R)-1--1-phenylpropan-2-ol

Guidance literature:: With sodium hydroxide; In methanol; at 20 ℃; for 0.5h;
DOI:10.1021/jm9910021

Reference yield:

: 255060-78-7
(-)-(1R,2S)-1-azido-1-phenyl-2-propanol

: 255060-81-2
(1R,2R)-1--1-phenylpropan-2-ol

Guidance literature:: Multi-step reaction with 4 steps

1: 79 percent / H₂; aq. HCl / 10 percent Pd/C / ethanol / 16 h / 2585.74 Torr

2: 86 percent / Et₃N / CH₂Cl₂ / 1 h / 20 °C

3: 25 percent / triphenylphosphine-cyclic sulfamide betaine / toluene / 17 h / 20 °C

4: 172 mg / aq. NaOH / methanol / 0.5 h / 20 °C

With hydrogenchloride; sodium hydroxide; triphenylphosphine-cyclic sulfamide betaine; hydrogen; triethylamine; palladium on activated charcoal; In methanol; ethanol; dichloromethane; toluene; 1: Reduction / 2: Acylation / 3: Esterification / 4: Hydrolysis;
DOI:10.1021/jm9910021