Benzyl Bromide → HCID 86672616, 화합물
반응식
[H-].[Na+].[CH3:3][O:4][C:5]1([O:16][CH3:17])[CH2:15][C:7]2([CH2:10][C:9]([CH2:13][OH:14])([CH2:11][OH:12])[CH2:8]2)[CH2:6]1.[CH2:18](Br)[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1.[Cl-].[NH4+]>O1CCCC1.CN(C)C=O>[CH2:18]([O:14][CH2:13][C:9]1([CH2:11][O:12][CH2:18][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[CH2:8][C:7]2([CH2:6][C:5]([O:4][CH3:3])([O:16][CH3:17])[CH2:15]2)[CH2:10]1)[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1참가 물질
실험 절차
Sodium hydride (755 mg, 17.3 mmol) was added to a dimethylformamide (40 ml)/tetrahydrofuran (20 ml) solution of the compound (1.56 g, 7.20 mmol) obtained in Step 1 above under ice cooling, the resulting mixture was stirred at room temperature for 10 minutes, then benzyl bromide (2.06 ml, 17.3 mmol) was added and the resulting mixture was stirred for 24 hours. Saturated ammonium chloride solution was added to the reaction mixture, followed by extraction with ethyl acetate. The organic layer was washed with brine and then dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure and the residue obtained was purified by silica gel column chromatography [n-hexane:ethyl acetate=4:1 (v/v)] to give 2.25 g (79%) of the title compound as an oil.
후처리
- stirringthe resulting mixture was stirred for 24 hours
- extractionfollowed by extraction with ethyl acetate
- washThe organic layer was washed with brine
- dry with materialdried over anhydrous sodium sulfate
- customThe solvent was evaporated under reduced pressure
- customthe residue obtained
- customwas purified by silica gel column chromatography [n-hexane:ethyl acetate=4:1 (v/v)]
출처 및 근거
- ORD 기록
- ord-b46e6a1895c04ccfb7c4ffd4f1291c19
- 출처 데이터셋
- uspto-grants-2014_01
- 특허 번호
- US08629133B2
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