HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 3-(Benzofuran-7-yloxy)-azetidine hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 1-Chloroethyl chloroformate | HCID 521305 | — |
| Reactant | 1-Benzhydryl-3-(benzofuran-7-yloxy)-azetidine | HCID 67154475 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(Benzofuran-7-yloxy)-azetidine hydrochloride | HCID 67154708 | 87.3% |
Reaction Steps
1-Chloroethyl chloroformate (107 μL, 0.99 mmol) was added to a solution of 1-benzhydryl-3-(benzofuran-7-yloxy)-azetidine (349 mg, 0.98 mmol) in dichloromethane (10 mL) at 0° C. The reaction mixture was stirred for 4 hours at room temperature. Ethanol (10 mL) was added and the reaction mixture was stirred for an additional 2 hours at room temperature and 3 hours at 40° C. After concentration to dryness, the residue was taken in a mixture dichloromethane/diethyl ether to afford the title compound as a white solid (193 mg, 87%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08846711B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-c6991bf548e74d89a02674fb435a9bdc |
| Source note | uspto-grants-2014_09 |