반응식
[CH2:1]([O:3][C:4]1[CH:9]=[CH:8][C:7]([F:10])=[CH:6][CH:5]=1)[CH3:2].CN(C)CCN(C)CCN(C)C.[Li]CCCC.CN([CH:31]=[O:32])C>C1COCC1>[CH2:1]([O:3][C:4]1[CH:5]=[CH:6][C:7]([F:10])=[C:8]([CH:9]=1)[CH:31]=[O:32])[CH3:2]참가 물질
반응 조건
- 온도
- -40 °C
실험 절차
To a solution of 1-ethoxy-4-fluorobenzene (1.1 g, 7.9 mmol) and pentamethyl diethylene triamine (2 mL) in anhydrous THF (6 mL) was added BuLi dropwise (1.38 M, 5.98 mL, 8.3 mmol) at −78° C. After addition, the reaction mixture was warmed up to −40° C. and stirred for 30 min, the reaction mixture was then cooled to −78° C. and DMF (0.7 mL) was added. The solution was warmed to rt, and stirred for 1 h. The reaction mixture was then partitioned between EtOAc and sat. NH4Cl, the organic layer was dried over (Na2SO4), filtered and concentrated. The residue was subjected to chromatographic purification (0-10% EtOAc/hexanes gradient), 600 mg (55%) of Intermediate 53.1 was obtained. 1H NMR (CDCl3) δ 1.40 (t, 3H), 4.08 (q, 2H), 6.81 (m, 1H), 7.15 (m, 1H), 7.29 (m, 1H), 10.33 (s, 1H).
후처리
- additionAfter addition
- temperaturethe reaction mixture was then cooled to −78° C.
- temperatureThe solution was warmed to rt
- stirringstirred for 1 h
- customThe reaction mixture was then partitioned between EtOAc and sat. NH4Cl
- dry with materialthe organic layer was dried over (Na2SO4)
- filtrationfiltered
- concentrationconcentrated
- customThe residue was subjected to chromatographic purification (0-10% EtOAc/hexanes gradient)
출처 및 근거
- ORD 기록
- ord-eb55b0b4a971477b89bb4b8cb59af4a6
- 출처 데이터셋
- uspto-grants-2009_08
- 특허 번호
- US07576098B2
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