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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 851370Generated: October 26, 2026

Acetic Acid → methyl 2-[(4R)-2-oxo-4-allylazetidin-1-yl]-3-methylbut-2-enoate

https://huagongshe.com/reaction/851370

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactantmethyl 2-[(4R)-3-bromo-4-allyl-2-oxoazetidin-1-yl]-3-methyl-2-butenoateHCID 54331335—
CatalystZincHCID 23994—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Productmethyl 2-[(4R)-2-oxo-4-allylazetidin-1-yl]-3-methylbut-2-enoateHCID 5432627328%

Reaction Conditions

Temperature5 °C

Reaction Steps

Methyl 2-[(4R)-3-bromo-4-allyl-2-oxoazetidin-1-yl]-3-methyl-2-butenoate (840 mg) was dissolved in methylene chloride (6 ml) and cooled to 5° C. To this cooled solution were added acetic acid (0.5 ml) and zinc powder (0.60 g), and the mixture was allowed to warm to room temperature. After stirring for 30 minutes, the reaction mixture was diluted with ethyl acetate (6 ml) and filtered through a pad of Celite. The filtrate was further diluted with ethyl acetate (50 ml) and washed successively with water, dilute sodium bicarbonate and brine. Drying over magnesium sulfate and evaporation left an oil, which was chromatographed on silica gel (20 g) eluting with a mixture of benzene and acetone (5:1) to give methyl 2-[(4R)-4-allyl-2-oxoazetidin-1-yl]-3-methyl-2-butenoate (174 mg) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04383945
Source datasetuspto-grants-1983_05
ORD IDord-0b89839265af48e291bccf0605770cdc
Source noteuspto-grants-1983_05