HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Chloroethyl chloroformate → Azetidin-3-yl(4-chlorophenyl)methanone hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Chloroethyl chloroformate | HCID 521305 | — |
| Reactant | (1-Benzhydryl-azetidin-3-yl)-(4-chloro-phenyl)-methanone | HCID 69361102 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Azetidin-3-yl(4-chlorophenyl)methanone hydrochloride | HCID 69358091 | — |
Reaction Steps
A solution of (1-Benzhydryl-azetidin-3-yl)-(4-chloro-phenyl)-methanone (19.8 g, 54.8 mmol) in dichloromethane (250 ml), cooled to −4° C., is treated with 1-chloroethylchloroformate (8.0 ml, 73.8 mmol) and allowed to warm to ambient temperature. The reaction mixture is stirred for 18 hours and then evaporated. The residue is dissolved in methanol (220 ml) and stirred at ambient temperature for 3.5 hours. The methanol solution is concentrated and the product precipitated by addition of diethylether. The precipitate is collected by filtration and dries under high vacuum to afford Azetidin-3-yl-(4-chloro-phenyl)-methanone hydrochloride. [MH]+ 195.95.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07288537B2 |
| Source dataset | uspto-grants-2007_10 |
| ORD ID | ord-650a3f69dbc245e8888a830ff0612043 |
| Source note | uspto-grants-2007_10 |