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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 851363Generated: November 2, 2026

Sodium Chloride → HCID 54067472, compound

https://huagongshe.com/reaction/851363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantSodium BicarbonateHCID 516892—
ReactantAG-G-75877HCID 11769254—
ReactantHCID 12959530HCID 12959530—
CatalystSilver tetrafluoroborateHCID 159722—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 54067472HCID 5406747279.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

Silver tetrafluoroborate (323 mg) was added to a stirred mixture of methyl 2-[(3S,4R)-4-chloro-2-oxo-3-phthalimidoazetidin-1-yl]-3-methylbut-2-enoate (500 mg) and methyl 3-(trimethylsilylmethyl)-but-3-enoate (460 mg) in dichloromethane (2.5 ml) at -78° C. under a nitrogen atmosphere. The stirring mixture was gradually allowed to warm to 0° C. during one hour and kept at 0° C. for 1.5 hours. A saturated aqueous sodium chloride (2 ml) was added and the heterogeneous mixture was brought to pH 7 with a saturated aqueous sodium bicarbonate. After stirring for 15 minutes, the mixture was diluted with ethyl acetate and filtered through a pad of Celite. The organic layer was separated, washed with brine, dried over magnesium sulfate, and evaporated. The residue was chromatographed on silica gel (10 g) eluting with a mixture of benzene and acetone (5:1). Further purification on a silica gel (10 g) eluting with 10-20% ethyl acetate in dichloromethane) afforded methyl 2-[(3R,4R)-4-[2-(methoxycarbonylmethyl)allyl]-2-oxo-3-phthalimidoazetidin-1-yl]-3-methylbut-2-enoate (483 mg) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04383945
Source datasetuspto-grants-1983_05
ORD IDord-d4140e057553473ab75a14a8a1695034
Source noteuspto-grants-1983_05