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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 867646Generated: October 30, 2026

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

https://huagongshe.com/reaction/867646

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 numberUS04775670
Source datasetuspto-grants-1988_10
ORD IDord-21362b46599a49a5879647e3952c8dc0
Source noteuspto-grants-1988_10