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Water → 2-Acetyl-6-methylphenyl cyclohexanecarboxylate

HRID 1200179
ノート
印刷プレビュー

反応式

HRID 1200179 の反応式
[C:1]([C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([CH3:10])[C:5]=1[OH:11])(=[O:3])[CH3:2].[CH:12]1([C:18](Cl)=[O:19])[CH2:17][CH2:16][CH2:15][CH2:14][CH2:13]1.O>N1C=CC=CC=1>[CH:12]1([C:18]([O:11][C:5]2[C:6]([CH3:10])=[CH:7][CH:8]=[CH:9][C:4]=2[C:1](=[O:3])[CH3:2])=[O:19])[CH2:17][CH2:16][CH2:15][CH2:14][CH2:13]1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 962WaterHCID 75938Cyclohexanecarbonyl chlorideHCID 2404371-(2-Hydroxy-3-methylphenyl)ethan-1-one

生成物 1

HCID 146504262-Acetyl-6-methylphenyl cyclohexanecarboxylate収率 100%

試薬・触媒・溶媒 1

HCID 1049Pyridine溶媒

実験手順

2-Acetyl-6-methylphenol (3.0 g) was dissolved in pyridine (15 ml) and to the solution was added dropwise cyclohexanecarbonyl chloride (3.08 g) with stirring at room temperature. After stirring for 4 hours, the reaction mixture was poured into cold water and extracted with ethyl acetate. The extract was washed with water, diluted hydrochloric acid and then water and dried (MgSO4). The solvent was distilled off under reduced pressure to obtain the title compound (5.2 g) as oil in a quantitative yield.

後処理

  1. stirringAfter stirring for 4 hours
  2. extractionextracted with ethyl acetate
  3. washThe extract was washed with water, diluted hydrochloric acid
  4. dry with materialwater and dried (MgSO4)
  5. distillationThe solvent was distilled off under reduced pressure

出典と根拠

ORDレコード
ord-0ef8405afcfb469ca191977d2c75a562
出典データセット
uspto-grants-1990_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04904690

反応ノート

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