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4-Methylenecyclohexylmethanol → 4-Methylidenecyclohexane-1-carbaldehyde

HRID 1388122
ノート
印刷プレビュー

反応式

HRID 1388122 の反応式
[Cr](O[Cr]([O-])(=O)=O)([O-])(=O)=O.[CH2:10]=[C:11]1[CH2:16][CH2:15][CH:14]([CH2:17][OH:18])[CH2:13][CH2:12]1>C(Cl)Cl>[CH2:10]=[C:11]1[CH2:16][CH2:15][CH:14]([CH:17]=[O:18])[CH2:13][CH2:12]1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 138604-MethylenecyclohexylmethanolHCID 24503Dichromate ion

生成物 1

HCID 158181364-Methylidenecyclohexane-1-carbaldehyde

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

反応条件

温度
60 °C

実験手順

To pydridinium dichromate (223 g., 0.59 mole) in 1 liter CH2Cl2, stirring under N2, was added dropwise 4-methylene-1-cyclohexanemethanol (50 g., 0.40 mole) in 75 ml. CH2Cl2 over a few minutes. After stirring for 21 hours at room temperature, the reaction mixture was heated at 60° C. for 24 hours. The reaction mixture was cooled, diluted with 400 ml. ether and decanted from solids. The solids were slurried with 400 ml. of fresh ether and decanted. The combined organic decants were filtered over fluorasil and diatomaceous earth and the filtrate concentrated in vacuo to an oil (41 g.) and distilled to yield title product, 13.6 g., b.p. 82°-90°/15-20 mm.

後処理

  1. stirringAfter stirring for 21 hours at room temperature
  2. temperatureThe reaction mixture was cooled
  3. additiondiluted with 400 ml
  4. customether and decanted from solids
  5. customof fresh ether and decanted
  6. customThe combined organic decants
  7. filtrationwere filtered over fluorasil and diatomaceous earth
  8. concentrationthe filtrate concentrated in vacuo to an oil (41 g.)
  9. distillationdistilled

出典と根拠

ORDレコード
ord-99b3c224b8e648508accf0939f44d860
出典データセット
uspto-grants-1984_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04430337

反応ノート

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