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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711439Generated: October 25, 2026

Benzyl chloroformate → (S)-2-Benzyloxycarbonylamino-3-(4-hydroxy-phenyl)-2-methyl-propionic acid methyl ester

https://huagongshe.com/reaction/1711439

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantSodium BicarbonateHCID 516892—
Reactant(S)-Methyl 2-amino-3-(4-hydroxyphenyl)-2-methylpropanoate hydrochlorideHCID 24847455—
SolventEthyl AcetateHCID 8857—
Product(S)-2-Benzyloxycarbonylamino-3-(4-hydroxy-phenyl)-2-methyl-propionic acid methyl esterHCID 66719336—

Reaction Steps

To a suspension of (S)-2-amino-3-(4-hydroxy-phenyl)-2-methyl-propionic acid methyl ester hydrochloride in ethyl acetate (25 mL) was added 1N NaHCO3 solution (12.5 ml.) and the mixture was stirred rapidly at ambient temperature for the addition of neat benzyl chloroformate (0.859 g, 1.01 eq., 5.05 mmol). Following addition, the reaction mixture was stirred for an additional hour; TLC and LC-MS analysis showed the reaction to be complete. The mixture was partitioned and the organic phase was separated and dried over Na2SO4 and concentrated. The crude product was used directly in the subsequent reaction without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790714B2
Source datasetuspto-grants-2010_09
ORD IDord-0ca141a42a8e46a89f1098e52a568903
Source noteuspto-grants-2010_09