Triethylamine → Methyl 4-(3-hydroxyanilino)-4-oxobutanoate

HRID 465133

反応式

HRID 465133 の反応式
[NH2:1][C:2]1[CH:3]=[C:4]([OH:8])[CH:5]=[CH:6][CH:7]=1.C(N(CC)CC)C.[C:16]([CH2:20][CH2:21][C:22](Cl)=[O:23])([O:18][CH3:19])=[O:17]>O1CCCC1>[OH:8][C:4]1[CH:3]=[C:2]([NH:1][C:22](=[O:23])[CH2:21][CH2:20][C:16]([O:18][CH3:19])=[O:17])[CH:7]=[CH:6][CH:5]=1

参加物

5

反応物 3

HCID 8471TriethylamineHCID 115683-AminophenolHCID 73888Butanoic acid, 4-chloro-4-oxo-, methyl ester

生成物 1

HCID 13491817Methyl 4-(3-hydroxyanilino)-4-oxobutanoate収率 88%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

To an ice cold solution of 3-aminophenol (21.8 g, 0.2 mol) and triethylamine (21.3 g, 0.2 mol) in tetrahydrofuran (250 ml) is added a solution of 3-carbomethoxypropanoyl chloride (30.1 g, 0.2 mol) in tetrahydrofuran. The reaction is allowed to warm to room temperature and is filtered through a pad of Celite and silica gel. The solvent is removed in vacuo to give a solid. Recrystallization from ethyl acetate gives 39.3 g (88% yield) of product, m.p. 144.5°-146° C.

後処理

  1. filtrationis filtered through a pad of Celite and silica gel
  2. customThe solvent is removed in vacuo
  3. customto give a solid
  4. customRecrystallization from ethyl acetate

出典と根拠

ORDレコード
ord-5584d776a8db4dcc8b6c5a6e6f45bfb2
出典データセット
uspto-grants-1985_10
特許番号
US04550172

関連ノート

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