참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sulfuric Acid | HCID 1118 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | HCID 13520354 | HCID 13520354 | — |
| 반응물 | Aluminium lithium hydride | HCID 21226445 | — |
| 반응물 | Aluminiumhydride | HCID 21584524 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Oxolane--water (1/1) | HCID 21881883 | — |
| 생성물 | 1-[1-(4-Bromophenyl)-2-(dimethylamino)ethyl]cyclohexanol | HCID 14183742 | — |
반응 단계
Lithium aluminum hydride (0.7 g) was suspended in dry THF (25 ml) cooled to 0° C. and concentrated sulfuric acid (0.5 ml) cautiously added in an in situ preparation of aluminum hydride. The mixture was stirred for one hour at 0° C. and the amide, 1-[(4-bromophenyl)[dimethylaminocarbonyl]methyl]cyclohexanol (4 g, 0.012 mole) was dissolved in THF (35 ml) and added rapidly dropwise. The reaction mixture was stirred at 0° C. for one hour. A THF-water mixture (1:1 v/v 6 ml) was added slowly followed by 10% sodium hydroxide (10 ml). The mixture was filtered and the residue washed well with ethyl acetate. The combined filtrate was dried over anhydrous potassium carbonate and evaporated to an oil (3.5 g) which was converted to the hydrochloride salt using 4 N isopropanolic HCl.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04761501 |
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| 출처 데이터셋 | uspto-grants-1988_08 |
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| ORD ID | ord-6caa22fbf96d454c889b849950738325 |
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| 출처 메모 | uspto-grants-1988_08 |
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