반응식
[C:1]1([C:7]([CH2:15][CH2:16][CH3:17])([CH2:12][CH2:13][CH3:14])[C:8]([O:10]C)=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1>O1CCCC1>[C:1]1([C:7]([CH2:15][CH2:16][CH3:17])([CH2:12][CH2:13][CH3:14])[C:8]([OH:10])=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1참가 물질
3
반응 조건
- 온도
- 25 °C
실험 절차
A solution of the product of Example 1B (7.63 g, 32.61 mmol) and potassium trimethylsilanoate (23.2 g of 90% material, 163 mmol) in tetrahydrofuran (163 mL) was warmed at reflux for 18 hours. The solution was cooled to 25° C. and concentrated in vacuo to remove the tetrahydrofuran. A solution of the residue in water (250 mL) was cooled to 0° C., and adjusted to pH 1 by addition of 4 N HCl solution. The resulting precipitate was collected by filtration, washed with water and dried to give the title compound (6.78 g, 95%). 1H NMR (300 MHz, CDCl3): δ 7.25 (m, 5 H), 1.99 (m, 4 H), 1.12 (m, 4 H), 0.90 (t, J=7.17 Hz, 6 H).
후처리
- temperatureat reflux for 18 hours
- concentrationconcentrated in vacuo
- customto remove the tetrahydrofuran
- temperatureA solution of the residue in water (250 mL) was cooled to 0° C.
- additionadjusted to pH 1 by addition of 4 N HCl solution
- filtrationThe resulting precipitate was collected by filtration
- washwashed with water
- customdried
출처 및 근거
- ORD 기록
- ord-8277ce1f669944fb9703e53b428dc2b6
- 출처 데이터셋
- uspto-grants-2009_05
- 특허 번호
- US07538105B2
연결된 노트
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