반응식
[CH3:1][CH2:2][CH2:3][CH2:4][CH:5]([OH:9])[C:6]([OH:8])=[O:7].[CH2:10](O)[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH3:19]>S(=O)(=O)(O)O>[OH:9][CH:5]([CH2:4][CH2:3][CH2:2][CH3:1])[C:6]([O:8][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH3:19])=[O:7]참가 물질
4
반응 조건
- 온도
- 140 °C
실험 절차
A 50 ml one neck round bottom flask equipped with a Dean Stark trap, condenser and a nitrogen inlet/outlet was charged with 5.0 g (0.038 moles) DL-2-hydroxycaproic acid, 23.95 g (0.151 moles) decyl alcohol, and 0.019 g sulfuric acid. The reactants were heated to 140° C. for 8 hours and water collected as the reaction proceeded. The acid was neutralized by washing three times with 50 ml saturated sodium bicarbonate solution. Approximately 50 ml ether was needed to break the emulsion. The organic layer was collected and dried over magnesium sulfate. Excess decyl alcohol was removed by high vacuum distillation to yield 4.34 g (49% yield) of clear colorless liquid. According to GC the product is 95.74% pure.
후처리
- customwater collected as the reaction
- washby washing three times with 50 ml saturated sodium bicarbonate solution
- customThe organic layer was collected
- dry with materialdried over magnesium sulfate
- customExcess decyl alcohol was removed by high vacuum distillation
출처 및 근거
- ORD 기록
- ord-07f892a4d3304c3596ab9f5fde776006
- 출처 데이터셋
- uspto-grants-1993_11
- 특허 번호
- US05260051
연결된 노트
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