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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 371214Generated: November 1, 2026

Trifluoroacetic acid → (3S-trans)-3-Benzyloxycarbonylamino-4-methylazetidinone

https://huagongshe.com/reaction/371214

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantAnisoleHCID 7519—
Reactanttert-Butyl ((2S,3S)-2-methyl-4-oxoazetidin-3-yl)carbamateHCID 13155285—
SolventDichloromethaneHCID 6344—
Product(3S-trans)-3-Benzyloxycarbonylamino-4-methylazetidinoneHCID 13182463—

Reaction Steps

A solution of 3.3 g of (3S-trans)-3-t-butoxycarbonylamino-4-methylazetidinone in 10 ml each of dichloromethane and anisole is cooled to 0° C. and 112 ml of trifluoroacetic acid is added. The solution is stirred for 90 minutes and evaporated in vacuo (benzene added and evaporated three times). The residue is dissolved in 70 ml of acetone and the solution is adjusted to pH 7 with 5% sodium bicarbonate solution. A total of 5.33 g of benzyl chloroformate is added over 1 hour at pH 6.5-7.5. The mixture is stirred for 30 minutes at pH 7, diluted with 100 ml of saturated salt, and extracted with ethyl acetate (three 400 ml portions). The residue obtained by evaporation is chromatographed on a 1 liter silica gel column. Elution with chloroform-ethyl acetate (4:1) gives 2.19 g of compound. Crystallization from ether-hexane yields 1.125 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04529698
Source datasetuspto-grants-1985_07
ORD IDord-e12f7d1de8ce405a84a00b45eb227dc6
Source noteuspto-grants-1985_07