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2,5-Dimethylphenol → HCID 54001442、化合物

HRID 1390942
ノート
印刷プレビュー

反応式

HRID 1390942 の反応式
[CH3:1][C:2]1[CH:3]=[C:4]([OH:9])[C:5](C)=[CH:6][CH:7]=1.[Cl-].[Al+3].[Cl-].[Cl-].Cl[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1>C1(C(C2C=CC=CC=2)CC(Cl)=O)C=CC=CC=1>[OH:9][C:4]1[CH:3]=[C:2]([CH3:1])[C:7]([C:2]([CH3:1])([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[CH2:3][C:4]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)=[O:9])=[CH:6][CH:5]=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 72672,5-DimethylphenolHCID 7964Chlorobenzene2 回HCID 6451240Aluminum(III) Chloride

生成物 1

HCID 54001442HCID 54001442、化合物

試薬・触媒・溶媒 1

HCID 30158933,3-Diphenylpropionyl chloride溶媒

実験手順

Twenty-four and four-tenths grams of 3,6-dimethylphenol and 26.6 grams of aluminum chloride are dissolved in 250 mls chlorobenzene and 48.9 grams of 3,3-diphenylpropionic acid chloride, dissolved in 150 mls chlorobenzene, are added while stirring. The stirring is continued for several days at 100° C. The chlorobenzene is evaporated in vacuo, the residue is mixed with ice and ether and washed several times with water. After drying with sodium sulfate, the ether is evaporated. Fifteen and one-tenth grams of 4-hydroxy-3,6-dimethyl-β,β-diphenylpropiophenone are obtained.

後処理

  1. additionare added
  2. waitThe stirring is continued for several days at 100° C
  3. customThe chlorobenzene is evaporated in vacuo
  4. additionthe residue is mixed with ice and ether
  5. washwashed several times with water
  6. dry with materialAfter drying with sodium sulfate
  7. customthe ether is evaporated

出典と根拠

ORDレコード
ord-35cc30991c614dca835ae308f304e07d
出典データセット
uspto-grants-1979_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04140770

反応ノート

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