HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 67154696, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 1-Chloroethyl chloroformate | HCID 521305 | — |
| Reactant | 1-Benzhydryl-3-(3-methylbenzofuran-2-yl)azetidine | HCID 67154654 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67154696 | HCID 67154696 | 62% |
Reaction Steps
To a cooled (0° C.) solution of 1-benzhydryl-3-(3-methylbenzofuran-2-yl)azetidine (52.0 mg, 0.147 mmol) in DCM (4 mL) under N2 was added 1-chloroethyl chloroformate (18.0 μL, 0.167 mmol) and the reaction was stirred at rt under N2 for 4 h. Next, EtOH was added and the mixture was stirred under nitrogen at 50° C. for 21 h. The mixture was concentrated in vacuo and the residue triturated with Et2O (3×5 mL), yielding the title product (20.4 mg, 62%) as an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08846711B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-a977df717deb41048c716c8ffdb6fad0 |
| Source note | uspto-grants-2014_09 |