반응식
[C:1]1([CH3:9])[CH:6]=[CH:5][C:4]([Mg]Br)=[CH:3][CH:2]=1.C(OCC)C.[CH3:15][Sn:16](Cl)([CH3:18])[CH3:17].[Cl-].[NH4+].CC1C=CC(C2C=CC(C)=CC=2)=CC=1>O1CCCC1.O>[CH3:9][C:1]1[CH:6]=[CH:5][C:4]([Sn:16]([CH3:18])([CH3:17])[CH3:15])=[CH:3][CH:2]=1참가 물질
실험 절차
41.4 L of 1.0M p-tolylmagnesium bromide in diethyl ether (41.4 mol) was added dropwise, maintaining the temperature below -5° C., over 4 hours to a solution of 546 g (2.79 mol) of trimethyltin chloride in tetrahydrofuran (4 L) under nitrogen at -10° C. The suspension was allowed to warm slowly to room temperature over 12 h then saturated ammonium chloride solution (1 L) was added followed by sufficient water (approximately 1 L) to dissolve the precipitate. The solution was extracted with ether-hexane (1:1) (1×4 L, 3×2 L). The combined organic phases were washed with brine, dried over magnesium sulfate and the solvents removed under vacuum. Purification by flash chromatography on silica gel, eluting with hexane/ethyl acetate (95:5), gave a pale yellow oil containing white crystals of 4,4'-dimethylbiphenyl which were removed by filtration to leave 711.3 g (100%) of product. 1H NMR (300 MHz, CDCl3): 0.30 (s 9H), 2.34 (s, 3H), 7.19 (d, 7.7 Hz, 2H), 7.40 (d, 7.7 Hz, 2H).
후처리
- temperaturemaintaining the temperature below -5° C.
- dissolutionto dissolve the precipitate
- extractionThe solution was extracted with ether-hexane (1:1) (1×4 L, 3×2 L)
- washThe combined organic phases were washed with brine
- dry with materialdried over magnesium sulfate
- customthe solvents removed under vacuum
- customPurification by flash chromatography on silica gel
- washeluting with hexane/ethyl acetate (95:5)
- customgave a pale yellow oil
- customwere removed by filtration
출처 및 근거
- ORD 기록
- ord-74a262af77854c29a7b53518fb9b4d76
- 출처 데이터셋
- uspto-grants-1996_12
- 특허 번호
- US05583130
연결된 노트
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