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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1771859Generated: November 3, 2026

Chloroacetyl chloride → 2-Chloro-1-(3-hydroxyazetidin-1-yl)ethan-1-one

https://huagongshe.com/reaction/1771859

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 66727974HCID 66727974—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product2-Chloro-1-(3-hydroxyazetidin-1-yl)ethan-1-oneHCID 90446601—

Reaction Steps

To a suspension of potassium carbonate (13.9 g, 100 mmol, 2.2 eq.) in water (33.5 mL) was added hydroxyazetidine hydrochloride (5 g, 45.6 mmol, 1 eq.). The reaction mixture was stirred at r.t. until complete dissolution, then diluted with 33.5 mL of DCM and cooled to 0° C. prior to the dropwise introduction of chloroacetyl chloride (4.4 mL, 54.8 mmol, 1.2 eq.) over 30 min After 2 h stirring at r.t., the reaction mixture was filtered, the organic layer was separated, and the aqueous phase was extracted with a mixture EtOAc/nBuOH 1:1 (6×16 mL). The combined organic layers were dried over Na2SO4, filtered and concentrated in vacuo. The residue was suspended in acetone (48 mL) and stirred vigorously for 20 min, filtered and the filtrate was concentrated in vacuo to afford Intermediate Gen-13-a.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249141B2
Source datasetuspto-grants-2016_02
ORD IDord-af6d8114cbc0451aa428869331784f15
Source noteuspto-grants-2016_02