Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Ethanol → 3-(2-(Thiophen-2-yl)ethoxy)azetidine hydrochloride
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Ethanol | HCID 702 | — |
| 반응물 | 1-Chloroethyl chloroformate | HCID 521305 | — |
| 반응물 | 1-Benzhydryl-3-(2-(thiophen-2-yl)ethoxy)azetidine | HCID 67154539 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 3-(2-(Thiophen-2-yl)ethoxy)azetidine hydrochloride | HCID 67154705 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08846711B2 |
| 출처 데이터셋 | uspto-grants-2014_09 |
| ORD ID | ord-8470f77bc3454ea2b731c5f16d4126ae |
| 출처 메모 | uspto-grants-2014_09 |