HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 3-(2-(Thiophen-2-yl)ethoxy)azetidine hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 1-Chloroethyl chloroformate | HCID 521305 | — |
| Reactant | 1-Benzhydryl-3-(2-(thiophen-2-yl)ethoxy)azetidine | HCID 67154539 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(2-(Thiophen-2-yl)ethoxy)azetidine hydrochloride | HCID 67154705 | — |
Reaction Steps
1-Chloroethylchloroformate (361 μL, 3.33 mmol) was added to a solution of 1-benzhydryl-3-(2-(thiophen-2-yl)ethoxy)azetidine (1.11 g, 3.17 mmol) in dichloromethane (15 mL) at room temperature. The reaction mixture was stirred overnight at room temperature, then 1 hour at 70° C. After cooling down to room temperature, ethanol (15 mL) was added and the reaction mixture was stirred at 70° C. for 1 hour. After concentration to dryness, the crude mixture was triturated in pentane (2×15 mL) to give a yellow oil (698 mg, quantitative) which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08846711B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-8470f77bc3454ea2b731c5f16d4126ae |
| Source note | uspto-grants-2014_09 |