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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2217144Generated: October 25, 2026

Carbon tetrabromide → N-Boc-beta-bromoalanine benzyl ester

https://huagongshe.com/reaction/2217144

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
ReactantBoc-Ser-OBzlHCID 7018792—
SolventDichloromethaneHCID 6344—
ProductN-Boc-beta-bromoalanine benzyl esterHCID 11772725—

Reaction Conditions

Temperature0 °C

Reaction Steps

The N-Boc-serine benzyl ester was brought up in dichloromethane (170 mL) and treated with carbon tetrabromide (26.37 g, 79.51 mmol, 1.2 eq.), and triphenylphosphine (25.20 g, 96.08 mmol, 1.45 eq.) and the solution was stirred at 0° C. for 30 min. The volatiles were then evaporated in vacuo and the residue was triturated with ether (1000 mL). The solid that separated out was filtered off and organic layer was evaporated in vacuo to get the crude product. The crude material was purified by flash chromatography on silica gel to get N-Boc-β-bromoalanine benzyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07407952B2
Source datasetuspto-grants-2008_08
ORD IDord-e5969927f6bd48ac9c7051628377c1da
Source noteuspto-grants-2008_08