Water → HCID 54500622, 화합물
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[CH3:1][CH:2]([CH2:4][CH2:5][CH2:6][C@H:7]([C@@H:9]1[C@:26]2([CH3:27])[C:12]([C:13]3[CH2:14][CH2:15][CH:16]4[C@:21]([C:23]=3[CH2:24][CH2:25]2)([CH3:22])[CH2:20][CH2:19][C@H:18](O)[CH2:17]4)=[CH:11][CH2:10]1)[CH3:8])[CH3:3].C(N(S(F)(F)F)CC)C.O>C(Cl)Cl>[CH3:3][CH:2]([CH2:4][CH2:5][CH2:6][C@H:7]([C@@H:9]1[C@:26]2([CH3:27])[C:12]([C:13]3[CH2:14][CH2:15][CH:16]4[C@:21]([C:23]=3[CH2:24][CH2:25]2)([CH3:22])[CH2:20][CH:19]=[CH:18][CH2:17]4)=[CH:11][CH2:10]1)[CH3:8])[CH3:1]참가 물질
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- 온도
- -78 °C
실험 절차
The title compound was prepared by using a method analogous to a method described in J Chemical Research (miniprint) (1979) 4714-4755. Cholesta-8,14-diene-3β-ol (1.17 g, 3 mmol) was dissolved in 10 ml of methylenechloride and cooled to −78° C. Over 10 min a solution of diethylaminosulfur trifluoride (1.4 g, 8,7 mmol) in 10 ml of methylenechloride was added at −78° C. The mixture was stirred and was then slowly heated to the room temperature. The reaction mixture was added 15 ml water while stirring was continued. The organic phase was separated and washed with 30 ml of 5% NaHCO3 and then with water. The organic phase was dried with MgSO4 and evaporated to dryness. The residue was purified by column chromatography using heptane for a first fraction A giving cholesta-2,8,14-triene, 0.23 g. Melting point: 104.7° C. Elementary analysis: Cal C: 88.45; H: 11.55. Found C: 88.58; H: 11.89. NMR: Hd: 5.64 (m 2H; C2—H; C3—H)d 5.35 (s,1H C 15H). Cd: 125.95 (C3), 125.67 (C2).
후처리
- temperaturewas then slowly heated to the room temperature
- stirringwhile stirring
- customThe organic phase was separated
- washwashed with 30 ml of 5% NaHCO3
- dry with materialThe organic phase was dried with MgSO4
- customevaporated to dryness
- customThe residue was purified by column chromatography
출처 및 근거
- ORD 기록
- ord-a31c490cfd394679a3e0a2d2f45f414a
- 출처 데이터셋
- uspto-grants-2003_11
- 특허 번호
- US06645953B2
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