참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Butanethiol | HCID 8012 | — |
| 반응물 | Dibutyl sulfide | HCID 11002 | — |
| 반응물 | Butyl methyl sulfide | HCID 12339 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 6-(6-Methoxy-2-naphthyl)-6-oxo-hexanoic acid | HCID 14425905 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 6-(6-Hydroxy-2-naphthyl)-6-oxohexanoic acid | HCID 13982541 | 79% |
반응 단계
Butyl sulfide was generated by placing NaH (2.57 g, 0.11 mol) in a 500 ml round bottom flask, adding butanethiol (5.14 ml, 0.48 mol) and stirring for 5 minutes. DMF (200 mls) was added and the reaction heated at reflux. Slowly, 6-(6-methoxy-2-naphthyl)-6-oxo-hexanoic acid (Example 5) (7.2 g, 0.25 mol) in DMF (100 ml) was added to the reaction and heated at reflux for 1 hour. The methyl butyl sulfide and DMF were vacuum distilled (7 torr, 28° C.) to leave a bright yellow powder that was dissolved in water and precipitated with 5% HCl. The precipitate was filtered, dissolved in ethyl acetate (1800 ml), dried (Na2SO4), filtered and evaporated to give a yellow solid that was recrystallized (ethyl acetate) to give the title compound (5.38 grams, 79% yield), mp 191-193° C.; MS, m/e 272 (M+).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04681894 |
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| 출처 데이터셋 | uspto-grants-1987_07 |
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| ORD ID | ord-44b9dc72756947e5b297b36a944c8769 |
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| 출처 메모 | uspto-grants-1987_07 |
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