참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Hydroxybenzyl Alcohol | HCID 125 | — |
| 반응물 | 1-(2-Methoxyphenyl)piperazine | HCID 1346 | — |
| 반응물 | Potassium Hydroxide | HCID 14797 | — |
| 반응물 | Lithium Bromide | HCID 82050 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 4-[[4-(2-Methoxyphenyl)piperazin-1-yl]methyl]phenol | HCID 1377149 | 56% |
반응 단계
4-Hydroxyphenyl methanol (124 g, 1 mole) and 192 g (1 mole) of 1-(2-methoxyphenyl)piperazine, together with 56 g (1 mole) of potassium hydroxide and 8.7 g (0.1 mole) of lithium bromide and 32.2 g (0.1 mole) of Aliquat 366 were dissolved in a mixture of 1 liter of toluene and 1 liter of water. The reaction mixture was refluxed for 24 hours, and then allowed to cool to room temperature. The organic layer was decanted and extracted twice with 500 ml of a 10% sodium hydroxide solution. The basic aqueous liquor was treated with ammonium acetate to provoke precipitation of the desired product. After filtration and drying under vacuum overnight at 50° C., 167 g (0.56 mole, 56% yield) of the title product was obtained as small white leaflets melting at 172° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05142052 |
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| 출처 데이터셋 | uspto-grants-1992_08 |
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| ORD ID | ord-0ebeb5b64dfb451d93a06df6381c57ed |
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| 출처 메모 | uspto-grants-1992_08 |
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