2-Ethoxybenzoyl chloride → 2-(2-Ethoxybenzamido)-6-methylbenzamide

HRID 412035ノート

反応式

HRID 412035 の反応式
[NH2:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]([CH3:11])[C:3]=1[C:4]([NH2:6])=[O:5].[CH2:12]([O:14][C:15]1[CH:23]=[CH:22][CH:21]=[CH:20][C:16]=1[C:17](Cl)=[O:18])[CH3:13]>N1C=CC=CC=1>[CH2:12]([O:14][C:15]1[CH:23]=[CH:22][CH:21]=[CH:20][C:16]=1[C:17]([NH:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]([CH3:11])[C:3]=1[C:4]([NH2:6])=[O:5])=[O:18])[CH3:13]

参加物

4

反応物 2

HCID 30163972-Ethoxybenzoyl chlorideHCID 167824692-Amino-6-methylbenzamide

生成物 1

HCID 185366002-(2-Ethoxybenzamido)-6-methylbenzamide

試薬・触媒・溶媒 1

HCID 1049Pyridine溶媒

実験手順

A mixture of 2-amino-6-methylbenzamide (UK Patent Application No 1,276,359; 5.49 g, 0.0365 mol), 2-ethoxybenzoyl chloride (7.67 g, 0.0415 mol) and pyridine (100 ml) was stirred at room temperature for 20 hours. The solvent was then removed by evaporation under vacuum and the residue dissolved in dichioromethane (200 ml). The solution was washed with saturated aqueous sodium carbonate solution (200 ml) and the aqueous phase back-extracted with further dichioromethane (2×100 ml). The organic solutions were combined, washed successively with 2N hydrochloric acid (3×100 ml) and brine (100 ml), then dried (Na2SO4) and evaporated under vacuum to give the title compound, which recrystallized from ethyl acetate as a colourless solid (6.86g, 63%), m.p. 166-168° C.

後処理

  1. customThe solvent was then removed by evaporation under vacuum
  2. dissolutionthe residue dissolved in dichioromethane (200 ml)
  3. washThe solution was washed with saturated aqueous sodium carbonate solution (200 ml)
  4. extractionthe aqueous phase back-extracted with further dichioromethane (2×100 ml)
  5. washwashed successively with 2N hydrochloric acid (3×100 ml) and brine (100 ml)
  6. dry with materialdried (Na2SO4)
  7. customevaporated under vacuum

出典と根拠

ORDレコード
ord-a2e6d412084e47c1b525007a4f0d7365
出典データセット
uspto-grants-2003_05
特許番号
US06562830B1

反応ノート

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