참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Palmitoyl chloride | HCID 8206 | — |
| 반응물 | 2-Dimethylaminopyridine | HCID 21885 | — |
| 반응물 | 6,7-Dihydroxy-2-methyl-4-thiaheptanoic acid t-butyl ester | HCID 10634448 | — |
| 용매 | Chloroform | HCID 6212 | — |
| 용매 | Triethylamine | HCID 8471 | — |
| 생성물 | 6,7-Bis(palmitoyloxy)-2-methyl-4-thiaheptanoic acid t-butyl ester | HCID 10532956 | 91% |
반응 단계
To a solution of 6,7-dihydroxy-2-methyl-4-thiaheptanoic acid t-butyl ester as obtained in Reference Example 40 (500 mg) in chloroform (30 ml), triethylamine (5.6 ml), palmitoyl chloride (5.50 g) and dimethylaminopyridine (5 mg) were added, followed by stirring at room temperature for 48 hours. After addition of water, the reaction mixture was extracted with ethyl acetate. The extract was washed with a 5% aqueous solution of citric acid, a saturated aqueous solution of sodium hydrogen carbonate and saturated saline, and dried over anhydrous sodium sulfate, and the solvent was distilled off. The resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:1) to yield the title compound (1.33 g, yield 91%) as a colorless oily substance.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05506267 |
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| 출처 데이터셋 | uspto-grants-1996_04 |
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| ORD ID | ord-3c15416e3e6e40ddadb81498e71cdeef |
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| 출처 메모 | uspto-grants-1996_04 |
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