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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1065834Generated: October 31, 2026

Acetic Anhydride → HCID 12795451, compound

https://huagongshe.com/reaction/1065834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 12795449HCID 12795449—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
ProductHCID 12795451HCID 12795451—

Reaction Steps

1 g of zinc powder is added in portions over a period of one hour to a solution, stirred under nitrogen and in an ice bath, of 380 mg (1 mmol) of 2-[(4R)-4-(benzthiazol-2-yldithio)-2-oxoazetidin-1-yl]-3-methylcrotonic acid methyl ester in 3 ml of acetic anhydride and 5 ml of glacial acetic acid. The reaction mixture is further stirred for one hour at room temperature, filtered and concentrated in vacuo. The residue is taken up in methylene chloride and washed in succession with 25% aqueous ammonium chloride solution and aqueous sodium bicarbonate solution. The combined aqueous phases are reextracted with methylene chloride, all the methylene chloride phases are combined, dried with sodium sulphate and concentrated in vacuo. The residue is chromatographed over 40 g of silica gel (deactivated with 10% water) with toluene and toluene/ethyl acetate (19:1) and yields the optically pure title compound having a melting point of 78°-80°; [α]D20 =+149°±1° (c= 1.007%; in CHCl3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04331676
Source datasetuspto-grants-1982_05
ORD IDord-5e630e514ad141679ad4b14a7c681e09
Source noteuspto-grants-1982_05