Methane → Octyl 2-hydroxy-4-(methylthio)butanoate

HRID 1754036

반응식

HRID 1754036 반응식
[OH:1][CH:2]([CH2:6][CH2:7][S:8][CH3:9])[C:3]([OH:5])=[O:4].C.[CH2:11](O)[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18].S([O-])(O)(=O)=O.[Na+]>O.C1(C)C=CC=CC=1>[OH:1][CH:2]([CH2:6][CH2:7][S:8][CH3:9])[C:3]([O:5][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18])=[O:4]

참가 물질

7

반응물 4

HCID 297MethaneHCID 9571-OctanolHCID 11427alpha-Hydroxy-gamma-methylmercaptobutyric acid2회HCID 516919Sodium Bisulfate

생성물 1

HCID 86689968Octyl 2-hydroxy-4-(methylthio)butanoate

시약·촉매·용매 2

HCID 962Water용매HCID 1140Toluene용매

실험 절차

To a multi-neck 5 L round bottom flask fitted with a mechanical stirrer, reflux condenser, and dean stark trap was added 2-hydroxy-4-(methylthio)butanoic acid (650 g, 4.33 mol, obtained for example by stirring Alimet over activated charcoal, filtering and concentrating in a rotovap), 1-octanol (845.4 g, 6.49 mol), sodium hydrogen sulfate (10.4 g, 86 mmol), and toluene (2.7 L).The resulting solution was heated to reflux with removal of water (˜146 mL) during the course of about 5.5 hours and the reaction was monitored by GC analysis. The reaction was cooled to room temperature overnight and then washed with saturated NaHCO3 (1×1.5 L), DI water (1×1.5 L) and brine (1×1.5 L), dried over sodium sulfate, filtered and evaporated to give a dark oil (1,525 g). The oil was purified by kugelrohr distillation at 130-150° C. and 0.1 mm Hg vacuum to give a pale yellow oil (507.6 g, 45%). m/z 285 (MNa+).

후처리

  1. customTo a multi-neck 5 L round bottom flask fitted with a mechanical stirrer
  2. temperaturereflux condenser, and dean stark trap
  3. filtrationfiltering
  4. temperaturewas heated
  5. washwashed with saturated NaHCO3 (1×1.5 L), DI water (1×1.5 L) and brine (1×1.5 L)
  6. dry with materialdried over sodium sulfate
  7. filtrationfiltered
  8. customevaporated

출처 및 근거

ORD 기록
ord-e62949eb12f340c0acc79a4bb205d34e
출처 데이터셋
uspto-grants-2015_10
특허 번호
US09169203B2

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