Triethylamine → 4-Methylbenzoic acid butyl ester

HRID 72090

反応式

HRID 72090 の反応式
I[C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][CH:3]=1.C(N([CH2:14][CH3:15])CC)C.CO[CH2:18][CH2:19][O:20][CH3:21].C([OH:26])CCC>CC([O-])=O.CC([O-])=O.[Pd+2]>[CH3:8][C:5]1[CH:6]=[CH:7][C:2]([C:21]([O:20][CH2:19][CH2:18][CH2:14][CH3:15])=[O:26])=[CH:3][CH:4]=1

参加物

5

反応条件

温度
95 °C

実験手順

Microencapsulated Pd(OAc)2 (prepared as described in Example 1, 0.23 g, 2 mol %, based on palladium content) was added to a solution of 4-iodotoluene (1 mmol) and triethylamine (4 mmol) in 1,2-Dimethoxyethane/n-butanol (1:1, 10 mL). The reaction vessel was evacuated and purged with carbon monoxide (CO). The reaction mixture was stirred at 95° C. for 24 h under a CO atmosphere (using a balloon). The mixture was allowed to cool to room temperature, diluted with dichloromethane (50 mL) and filtered through a polyethylene frit (20-micron porosity). The filtrate was washed with water (2×20 mL) and dried (MgSO4). Evaporation under reduced pressure and purification by column chromatography gave butyl 4-methylbenzoate, 89%; IR: 1714; 1H NMR (400 MHz; CDCl3): 7.93 (2H, d, J 8.2), 7.23 (2H, d, J 8), 4.31 (2H, t, J 6.6), 2.41 (3H, s), 1.78-1.71 (2H, m), 1.49 (2H, sext, J 7.5) and 0.98 (3H, t, J 7.4); 13C NMR (CDCl3): 167.2, 143.8, 130.0, 129.4, 128.2, 65.0, 31.2, 22.0, 19.7 and 14.1.

後処理

  1. customThe reaction vessel was evacuated
  2. custompurged with carbon monoxide (CO)
  3. temperatureto cool to room temperature
  4. additiondiluted with dichloromethane (50 mL)
  5. filtrationfiltered through a polyethylene frit (20-micron porosity)
  6. washThe filtrate was washed with water (2×20 mL)
  7. dry with materialdried (MgSO4)
  8. customEvaporation
  9. customunder reduced pressure and purification by column chromatography

出典と根拠

ORDレコード
ord-f2f189b83bd44c17989fa8f5dc856a5a
出典データセット
uspto-grants-2014_09
特許番号
US08828902B2

関連ノート

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