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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389863Generated: October 30, 2026

Hydrochloric Acid → (S)-1-(4-Chloro-phenyl)-azetidine-2-carboxylic acid

https://huagongshe.com/reaction/389863

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactantp-BromochlorobenzeneHCID 7806—
ReactantL-Azetidine-2-carboxylic acidHCID 16486—
CatalystCopper iodideHCID 83717—
SolventDimethylacetamideHCID 31374—
Product(S)-1-(4-Chloro-phenyl)-azetidine-2-carboxylic acidHCID 67284015—

Reaction Conditions

Temperature110 °C

Reaction Steps

A sealed tube is charged with (S)-Azetidine-2-carboxylic acid; hydrochloride (2 g; 19.8 mmol), 4-bromochlorobenzene (3.8 g; 19.8 mmol) and copper iodide (I) (0.38 g; 1.99 mmol) is evacuated and back-filled with Argon 3 times. Dimethylacetamide (40 mL) is added and the tube is sealed and purged with Argon and evacuated 3 times. The sealed tube is heated in 110° C. oil bath for 72 hours. After this time, the reaction mixture is cooled to room temperature and partitioned between ethyl acetate and water. The organic layer is discarded. The aqueous layer is acidified to PH˜1 by adding 1N hydrochloric acid and then extracted with ethyl acetate twice. The organics are combined and washed with brine, dried over Na2SO4, filtered and concentrated in vacuo. Purification by flash chromatography on silica gel using methanol/methylene chloride provides the title compound, m/z 212 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383615B2
Source datasetuspto-grants-2013_02
ORD IDord-6afbc2057c354a3cbee3a4cf940605c2
Source noteuspto-grants-2013_02