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Ethyl Bromide → 4-Acetyl-4'-ethoxybiphenyl

HRID 1608748
ノート
印刷プレビュー

反応式

HRID 1608748 の反応式
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:13]=[CH:12][C:11]([C:14](=[O:16])[CH3:15])=[CH:10][CH:9]=2)=[CH:4][CH:3]=1.[CH2:17](Br)[CH3:18].C(=O)([O-])[O-].[K+].[K+].C1(=O)CCCCC1>>[CH2:17]([O:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[CH:13]=[CH:12][C:11]([C:14](=[O:16])[CH3:15])=[CH:10][CH:9]=2)=[CH:6][CH:7]=1)[CH3:18]
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 4

HCID 6332Ethyl BromideHCID 7967CyclohexanoneHCID 11430Potassium CarbonateHCID 103308064-(4-Acetylphenyl)phenol

生成物 1

HCID 232504334-Acetyl-4'-ethoxybiphenyl

実験手順

A reaction vessel was charged with 230 g of 4-hydroxy-4'-acetylbiphenyl, 164 g of ethyl bromide, 276 g of potassium carbonate and 1.7 l of cyclohexanone. The mixture was reacted together under agitation for 3 hours at 65°-70° C. and then for 6 hours at 95°-100° C. The reaction liquid was filtered and the resultant solid matter was washed with benzene. The filtrate and the washing liquid were combined, washed with water and dried over Glauber's salt, The solvents were distilled off and the residue was recrystallized from a mixed solvent of acetone-methanol to obtain 4-ethoxy-4'-acetylbiphenyl.

後処理

  1. customThe mixture was reacted together under agitation for 3 hours at 65°-70° C.
  2. customThe reaction liquid
  3. filtrationwas filtered
  4. washthe resultant solid matter was washed with benzene
  5. washwashed with water
  6. dry with materialdried over Glauber's salt
  7. distillationThe solvents were distilled off
  8. customthe residue was recrystallized from a mixed solvent of acetone-methanol

出典と根拠

ORDレコード
ord-908052fa35794ecbae223747716a08f4
出典データセット
uspto-grants-1995_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05397504

反応ノート

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