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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 523860Generated: November 2, 2026

Benzyl chloroformate → (2S)-4-[[3-carboxy-3-(phenylmethoxycarbonylamino)propyl]disulfanyl]-2-(phenylmethoxycarbonylamino)butanoic acid

https://huagongshe.com/reaction/523860

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantSodium HydroxideHCID 14798—
ReactantL-HomocystineHCID 439579—
SolventTetrahydrofuranHCID 8028—
Product(2S)-4-[[3-carboxy-3-(phenylmethoxycarbonylamino)propyl]disulfanyl]-2-(phenylmethoxycarbonylamino)butanoic acidHCID 320239—

Reaction Conditions

Temperature7.5 °C

Reaction Steps

L-Homocystine (200.0 g, 745.5 mmol, 1.0 eq.) is suspended in THF (1000 mL, 5.0 vol.) and cooled to 5-10° C. Addition of 20% sodium hydroxide (521.7 mL, 626.2 g, 125.25 g at 100%, 3.13 mmol, 4.2 eq.) is followed by addition of benzyl chloroformate (220.3 mL, 267 g, 1565.5 mmol, 2.1 eq.). Conversion is complete after a night at room temperature (L-Homocystine<1%). Extractions and washings of the organic layer with water leads to a yellow oil which is isolated in quantitative yield, and which slowly crystallizes as a yellowish solid at room temperature.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340497B2
Source datasetuspto-grants-2016_05
ORD IDord-565d4e98442e4fa395f21ea922aa76b5
Source noteuspto-grants-2016_05