참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methanol | HCID 887 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | Ethyl 1-[2-bis(4-fluorophenyl)methoxyethyl]-4-piperidinecarboxylate | HCID 10069740 | — |
| 반응물 | Diisobutylaluminumhydride | HCID 21225700 | — |
| 용매 | Toluene | HCID 1140 | — |
| 용매 | Hexane | HCID 8058 | — |
| 생성물 | HCID 9975721 | HCID 9975721 | 91.5% |
반응 단계
3.03 g of ethyl 1-[2-bis(4-fluorophenyl)methoxyethyl]-4-piperidinecarboxylate (prepared as described in preparation 8) were dissolved in 30 ml of toluene, under a stream of nitrogen, and the resulting solution was cooled at -68° C. 8.2 ml of a 1M solution of diisobutylaluminum hydride in hexane was then added dropwise to the cooled mixture over a period of 10 minutes, and the mixture was stirred for 1 hour at -68° C. At the end of this time, 2 ml of methanol and 3 ml of a saturated aqueous solution of ammonium chloride were added to the reaction solution. The mixture was then extracted with ethyl acetate, to give 2.47 g (yield 91%) of the title compound as an oil, whose properties were the same as those of the product of step (a).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05294623 |
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| 출처 데이터셋 | uspto-grants-1994_03 |
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| ORD ID | ord-cbe09b54350b4e8787548fce94d652ef |
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| 출처 메모 | uspto-grants-1994_03 |
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