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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 843282Generated: October 31, 2026

Hydrochloric Acid → (2R,3S)-3-(t-butoxycarbonyl)amino-4-phenyl-butane-1,2-diol

https://huagongshe.com/reaction/843282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium borohydrideHCID 4311764—
ReactantN-tert-butoxycarbonyl-3(S)-amino-2(R)-hydroxy-4-phenylbutyric acid methyl esterHCID 11449720—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product(2R,3S)-3-(t-butoxycarbonyl)amino-4-phenyl-butane-1,2-diolHCID 1107687072.6%

Reaction Conditions

Temperature20 °C

Reaction Steps

A solution of N-tert-butoxycarbonyl-3(S)-amino-2(R)-hydroxy-4-phenylbutyric acid methyl ester 99 g dissolved in ethanol 130 ml was kept at 15-25° C. and mixed with sodium borohydride 15.7 g and stirred at 15-25° C. for 2.5hrs. The reaction solution was diluted with water, adjusted with 6N-HCl to pH 2.5-3.5 and thereafter the solvent was distilled away to half the volume of the resultant solution, and then ethyl acetate was added to the solution. The solution thus obtained was washed with water and aqueous 10% sodium chloride solution successively to separate an organic phase. The solvent in the organic phase was distilled away and then ethyl acetate was added to the resultant concentrated solution to cool it and n-heptane was added to the solution halfway. Further n-heptane was added to the cloudy solution obtained. Thereafter, the solution was stirred at 10° C. to deposit crystals, which were filtered and dried in vacuum to obtain the N-tert-butoxycarbonyl-3(S)-amino-2(R)-hydroxy-4-phenyl-1-butanol(65.4 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06376685B1
Source datasetuspto-grants-2002_04
ORD IDord-25f50bf5216e4d03ad277b2ecf42a8c8
Source noteuspto-grants-2002_04