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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 843283Generated: October 31, 2026

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

https://huagongshe.com/reaction/843283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
ReactantN-tert-butoxycarbonyl-3(S)-amino-2(R)-hydroxy-4-phenylbutyric acid methyl esterHCID 11449720—
SolventEthanolHCID 702—
Product(2R,3S)-3-(t-butoxycarbonyl)amino-4-phenyl-butane-1,2-diolHCID 11076870—

Reaction Conditions

Temperature30 °C

Reaction Steps

A solution of N-tert-butoxycarbonyl-3(S)-amino-2(R)-hydroxy-4-phenylbutyric acid methyl ester 154.7 g dissolved in ethanol 300 ml was kept at 5-15° C. and mixed with sodium borohydride 24.6 g and stirred at 15-45° C. for 3hrs. The reaction solution was cooled and adjusted with 3N-HCl to pH 2.5-3.5. Water was added to the resultant solution and then the obtained solution was cooled to 5° C. or lower to deposit crystals. The crystals were filtered, dissolved in ethyl acetate, and washed with aqueous 5% sodium bicarbonate solution to separate an organic phase, which was washed with aqueous 10% sodium chloride solution and concentrated under an reduced pressure to obtain the crude N-tert-butoxycarbonyl-3(S)-amino-2(R)-hydroxy-4-phenyl-1-butanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06376685B1
Source datasetuspto-grants-2002_04
ORD IDord-cc979490d8a7469887043eb97502b186
Source noteuspto-grants-2002_04