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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1381206Generated: November 1, 2026

Dichloromethane → (4-Allylthio-3-ethylazetidin-2-on-1-yl)acetic acid

https://huagongshe.com/reaction/1381206

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantPotassium HydroxideHCID 14797—
ReactantMethyl (4-allylthio-3-ethylazetidin-2-on-1-yl)acetateHCID 13106494—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product(4-Allylthio-3-ethylazetidin-2-on-1-yl)acetic acidHCID 1310649690.6%

Reaction Steps

To a stirred solution of 3 g of methyl 2-(4-allylthio-3-ethylazetidin-2-on-1-yl)acetate in 10 ml of absolute ethanol was added dropwise a solution of 0.9 g of potassium hydroxide in a mixture of 12 ml of ethanol and 1 ml of water. After 5 minutes, the mixture was poured into a mixture of 10 ml of dichloromethane and 20 ml of water. After acidification with 13 ml of 2M HCl, the mixture was extracted with further dichloromethane; the dichloromethane extracts were extracted with saturated sodium bicarbonate solution. These aqueous extracts were acidified to pH 1.5 with 5M HCl and then extracted with dichloromethane. These organic extracts were evaporated to dryness to afford the title compound as a white crystalline solid (2.56 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04585767
Source datasetuspto-grants-1986_04
ORD IDord-f12a6389ce874b389f99ac0dc46f6671
Source noteuspto-grants-1986_04