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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 371215Generated: October 31, 2026

Dimethylformamide → Tetrabutylammonium (2S,3S)-3-{[(benzyloxy)carbonyl]amino}-2-methyl-4-oxoazetidine-1-sulfonate

https://huagongshe.com/reaction/371215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSulfur trioxideHCID 24682—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant(3S-trans)-3-Benzyloxycarbonylamino-4-methylazetidinoneHCID 13182463—
ProductTetrabutylammonium (2S,3S)-3-{[(benzyloxy)carbonyl]amino}-2-methyl-4-oxoazetidine-1-sulfonateHCID 13631608—

Reaction Steps

A solution of 600 mg of (3S-trans)-3-benzyloxycarbonylamino-4-methylazetidinone in 2 ml of dimethylformamide is cooled to 0° C. and 4 ml of 0.8M sulfur trioxide in dimethylformamide is added. The solution is stirred at room temperature under nitrogen for 1 hour and poured into 80 ml of cold 0.5M monobasic potassium phosphate (adjusted to pH 5.5). The solution is extracted with three 50 ml portions of methylene chloride (discarded) and 868 mg of tetrabutylammonium bisulfate is added. The resulting solution is extracted with four 75 ml portions of methylene chloride. The combined organic layer is washed with 8% aqueous sodium chloride, dried, and evaporated in vacuo yielding 1.54 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04529698
Source datasetuspto-grants-1985_07
ORD IDord-074ef26fcc2f4838b3808cf015162527
Source noteuspto-grants-1985_07