참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methane | HCID 297 | — |
| 반응물 | Stearyl Alcohol | HCID 8221 | — |
| 반응물 | alpha-Hydroxy-gamma-methylmercaptobutyric acid | HCID 11427 | — |
| 반응물 | Sodium Bisulfate | HCID 516919 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | Octadecyl 2-hydroxy-4-(methylthio)butanoate | HCID 86689973 | — |
반응 단계
To a 3 neck 3 L round bottom flask fitted with a reflux condenser, dean stark trap, thermocouple, and mechanical overhead stirrer was added 2-hydroxy-4-(methylthio)butanoic acid (130 g, 870 mmol, obtained by stirring Alimet over activated charcoal, filtering and concentrating in a rotovap), 1-octadecanol (351.2 g, 1.30 mol), sodium hydrogen sulfate (2.10 g, 17 mmol), and toluene (1000 mL). The reaction was heated to reflux with removal of water (21.5 mL) during the course of about 4 hours. The reaction was cooled to room temperature overnight and the mixture was filtered. The filtrate was washed with saturated NaHCO3 (1×500 mL), DI water (1×500 mL) and brine (1×500 mL), dried over sodium sulfate, filtered and evaporated to give light brown semi-solid (319.4 g). The semi-solid was treated with hexanes (750 mL) and the resulting mixture was filtered. The solid was washed with hexanes (250 mL) and the combined filtrate was evaporated to give an oil which solidified upon standing (278.8 g). The solid was purified by kugelrohr at 175° C. and 0.1 mm Hg vacuum to give a waxy solid remaining in the distillation pot (214.0 g, 61%). m/z 425 (MNa+).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09169203B2 |
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| 출처 데이터셋 | uspto-grants-2015_10 |
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| ORD ID | ord-aff56a75d5bf4fa4a032f5ad9d629bad |
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| 출처 메모 | uspto-grants-2015_10 |
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