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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2309082Generated: October 31, 2026

Benzene → HCID 86741780, compound

https://huagongshe.com/reaction/2309082

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantAcetyl bromideHCID 10482—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 56614980HCID 56614980—
SolventDimethylformamideHCID 6228—
ProductHCID 86741780HCID 86741780—

Reaction Steps

A solution of 687 mg (1.29 mmole) of 2-[(3S,4R)-4-(benzthiazol-2-yldithio)-3-phenoxyacetoxy-2-oxoazetidin-1-yl]-3-methylcrotonic acid methyl ester in 14 ml of dimethylformamide is added to a solution, cooled to -20°, of 76 mg (2 mmole) of sodium borohydride in 10 ml of dimethylformamide and the mixture is stirred at the same temperature for 10 minutes. 7 ml of freshly distilled acetyl bromide are added to the reaction mixture, which is further stirred at 0° for 40 minutes. After adding 400 ml of benzene, the reaction mixture is washed in succession with aqueous sodium bicarbonate solution, water and sodium chloride solution, dried over sodium sulphate and concentrated by evaporation in vacuo. After chromatography over silica gel with toluene/ethyl acetate (19:1) the residue yields the title compound in the form of an oil, which is further purified on silica gel plates with toluene/ethyl acetate (4:1). The title compound is obtained in oily form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04692442
Source datasetuspto-grants-1987_09
ORD IDord-f87edf64806b48a3833bfd648421e3cd
Source noteuspto-grants-1987_09