참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1,2-Dichloroethane | HCID 11 | — |
| 반응물 | 1-Chloroethyl chloroformate | HCID 521305 | — |
| 반응물 | 1-(Diphenylmethyl)-3-(2-thienylmethoxy)azetidine | HCID 67154602 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | 3-(2-Thienylmethoxy)azetidine hydrochloride | HCID 67154544 | — |
반응 단계
A 50 mL flask was charged with 1-(diphenylmethyl)-3-(2-thienylmethoxy)azetidine (204 mg, 0.61 mmol; which may be prepared as described in Step 2) and 1,2-dichloroethane (2.7 mL). 1-Chloroethyl chloroformate (86 μL, 0.79 mmol) was added and the reaction mixture was stirred at 70° C. for 1.5 h. After cooling to room temperature, methanol (2.7 mL) was added and the reaction mixture was stirred at 70° C. for 1.5 h. The reaction mixture was concentrated to dryness. The crude mixture was triturated in pentane to give a dark wax (140 mg, quantitative) which was used without further purification.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09051321B2 |
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| 출처 데이터셋 | uspto-grants-2015_06 |
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| ORD ID | ord-1b19963750ac4979891e4080cf839359 |
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| 출처 메모 | uspto-grants-2015_06 |
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