반응식
[CH3:1][O:2][C:3](=[O:15])[C:4]1[CH:9]=[CH:8][C:7]([C:10](OC)([CH3:12])[CH3:11])=[CH:6][CH:5]=1.[CH2:16]([Si](C)(C)C)[CH:17]=C.[CH2:23](Cl)Cl>Cl[Ti](Cl)(Cl)Cl>[CH3:1][O:2][C:3](=[O:15])[C:4]1[CH:9]=[CH:8][C:7]([C:10]([CH3:23])([CH3:12])[CH2:11][CH:16]=[CH2:17])=[CH:6][CH:5]=1참가 물질
반응 조건
- 온도
- -78 °C
실험 절차
827 mg of 4-(1-methoxy-1-methyl-ethyl)-benzoic acid methyl ester (3.97 mmol) (prepared as described in example S102) and 1.26 ml allyltrimethylsilane (7.94 mmol) were dissolved in 10 ml DCM and the solution was cooled to −78° C. Then 4.77 ml of a 1 M solution of TiCl4 in DCM were added dropwise. After 30 h the reaction was quenched at −78° C. by addition of methanol. Then water was added and the mixture was extracted 3 times with DCM. The combined extracts were washed with brine, dried with magnesium sulfate, filtered and concentrated. The remaining residue was purified by chromatography (silica gel; cyclohexane/EtOAc 95:5) to give 331 mg (38%) of 4-(1,1-dimethyl-but-3-enyl)-benzoic acid methyl ester as a colorless liquid. 1H NMR (CDCl3, 300 MHz): δ 1.33 (s, 6H), 2.38 (d, J=7 Hz, 2H), 3.90 (s, 3H), 4.91-5.00 (m, 3H), 5.51 (m, 1H), 7.41 (d, J=9 Hz, 1H), 7.97 (d, J=9 Hz, 1H).
후처리
- customAfter 30 h the reaction was quenched at −78° C. by addition of methanol
- additionThen water was added
- extractionthe mixture was extracted 3 times with DCM
- washThe combined extracts were washed with brine
- dry with materialdried with magnesium sulfate
- filtrationfiltered
- concentrationconcentrated
- customThe remaining residue was purified by chromatography (silica gel; cyclohexane/EtOAc 95:5)
출처 및 근거
- ORD 기록
- ord-7452562ce91a4b45a012e10bbdf46c86
- 출처 데이터셋
- uspto-grants-2007_08
- 특허 번호
- US07259183B2
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