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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | p-Bromochlorobenzene | HCID 7806 | — |
| Reactant | L-Azetidine-2-carboxylic acid | HCID 16486 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | (S)-1-(4-Chloro-phenyl)-azetidine-2-carboxylic acid | HCID 67284015 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08383615B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-6afbc2057c354a3cbee3a4cf940605c2 |
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| Source note | uspto-grants-2013_02 |
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