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Pyridine → (4-Oxo-1-phenylcyclohexyl)methyl acetate

HRID 1576216
ノート
印刷プレビュー

反応式

HRID 1576216 の反応式
[OH:1][CH2:2][C:3]1([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[CH2:8][CH2:7][C:6](=[O:9])[CH2:5][CH2:4]1.N1C=CC=CC=1.[C:22](OC(=O)C)(=[O:24])[CH3:23]>O>[C:22]([O:1][CH2:2][C:3]1([C:10]2[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=2)[CH2:4][CH2:5][C:6](=[O:9])[CH2:7][CH2:8]1)(=[O:24])[CH3:23]
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 1049PyridineHCID 7918Acetic AnhydrideHCID 215146764-(Hydroxymethyl)-4-phenylcyclohexan-1-one

生成物 1

HCID 21514685(4-Oxo-1-phenylcyclohexyl)methyl acetate収率 35.8%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

6.6 g. of 4-hydroxymethyl-4-phenylcyclohexanone is dissolved in 40 ml. of pyridine and 20 ml. acetic anhydride. After about 20 hours of standing at room temperature, the mixture is poured into ice and water. The gum that precipitates is extracted with ether. The organic layer is washed successively with water, 2.5 N hydrochloric acid, water, sodium bicarbonate solution, and brine, and then evaporated to dryness. The solid residue is recrystallized from Skellysolve B to give 6.74 g. (35.8% yield) of 4-acetoxymethyl-4-phenylcyclohexanone, having a melting point of 74° to 79°C.

後処理

  1. customThe gum that precipitates
  2. extractionis extracted with ether
  3. washThe organic layer is washed successively with water, 2.5 N hydrochloric acid, water, sodium bicarbonate solution, and brine
  4. customevaporated to dryness
  5. customThe solid residue is recrystallized from Skellysolve B
  6. customto give 6.74 g

出典と根拠

ORDレコード
ord-ebf73aacd42445a5a9b53afbcc3f23c5
出典データセット
uspto-grants-1976_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US03979444

反応ノート

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