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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016612Generated: November 1, 2026

Acetic Anhydride → HCID 13242805, compound

https://huagongshe.com/reaction/1016612

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 13242803HCID 13242803—
SolventFormic AcidHCID 284—
SolventDichloromethaneHCID 6344—
ProductHCID 13242805HCID 1324280591%

Reaction Steps

A solution of 2-(R,S)-benzyl-3-benzyloxyamino-propionic acid (7.8 g, 27.4 mmol) in formic acid (40 mL) was cooled in an ice-water bath and treated dropwise with acetic anhydride (15 mL). The reaction was allowed to warm to room temperature and stirred for 18 hours. The reaction mixture was diluted with dichloromethane (150 mL) and partitioned with water (100 mL). The organic layer was separated, washed with brine, dried over magnesium sulphate, filtered and concentrated under reduced pressure to yield 2-(R,S)-benzyl-3-(benzyloxy-formyl-amino)-propionic acid as a colourless oil (7.8 g, 91%). 1H-NMR; δ (CDCl3), 7.87-7.16 (10H, m), 4.924.66 (2H, m), 4.03-3.90 (2H, m), 3.17-2.93 (2H, m), 2.78-2.70 (1H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06476067B1
Source datasetuspto-grants-2002_11
ORD IDord-0db83764ced841e0818303521a93807a
Source noteuspto-grants-2002_11