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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1715619Generated: November 2, 2026

Carbon tetrabromide → Methyl (S)-2-(Boc-amino)-4-bromobutyrate

https://huagongshe.com/reaction/1715619

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
ReactantMethyl N-(tert-butoxycarbonyl)-L-homoserinateHCID 10561607—
SolventDichloromethaneHCID 6344—
ProductMethyl (S)-2-(Boc-amino)-4-bromobutyrateHCID 1068532876%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cooled (0° C.) solution of (S)-2-tert-butoxycarbonylamino-4-hydroxy-butyric acid methyl ester (28.7 g, 123 mmol) in dichloromethane (500 mL) was added CBr4 (51.0 g, 154 mmol). The mixture was stirred for 5 minutes before the portion-wise addition of triphenylphosphine (48.41 g, 185 mmol). The mixture continued to stir at 0° C. for 1 hour and was then allowed to warm to room temperature. The solvent was removed under reduced pressure and was then diluted with ether (500 mL) and stirred for 30 minutes. The mixture was filtered, and the filtrate was concentrated under reduced pressure. The residue was chromatographed eluting with ether/hexanes (1:2) to afford 27.5 g of white solid (76% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799782B2
Source datasetuspto-grants-2010_09
ORD IDord-809b16ba470f46feb72210ac58e7d91a
Source noteuspto-grants-2010_09