Diethyl Ether → Stannane, trimethyl(4-methylphenyl)-

HRID 1080722

反応式

HRID 1080722 の反応式
[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]=1

参加物

8

実験手順

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).

後処理

  1. temperaturemaintaining the temperature below -5° C.
  2. dissolutionto dissolve the precipitate
  3. extractionThe solution was extracted with ether-hexane (1:1) (1×4 L, 3×2 L)
  4. washThe combined organic phases were washed with brine
  5. dry with materialdried over magnesium sulfate
  6. customthe solvents removed under vacuum
  7. customPurification by flash chromatography on silica gel
  8. washeluting with hexane/ethyl acetate (95:5)
  9. customgave a pale yellow oil
  10. customwere removed by filtration

出典と根拠

ORDレコード
ord-74a262af77854c29a7b53518fb9b4d76
出典データセット
uspto-grants-1996_12
特許番号
US05583130

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