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Pyridine → 1-(4-Bromophenyl)-2-p-tolylethane-1,2-dione

HRID 1834869
ノート
印刷プレビュー

反応式

HRID 1834869 の反応式
N1C=CC=CC=1.[Br:7][C:8]1[CH:13]=[CH:12][C:11]([C:14]([CH:16]([C:18]2[CH:23]=[CH:22][C:21]([CH3:24])=[CH:20][CH:19]=2)[OH:17])=[O:15])=[CH:10][CH:9]=1>O>[Br:7][C:8]1[CH:13]=[CH:12][C:11]([C:14]([C:16]([C:18]2[CH:19]=[CH:20][C:21]([CH3:24])=[CH:22][CH:23]=2)=[O:17])=[O:15])=[CH:10][CH:9]=1
参加物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 1049PyridineHCID 203722961-(4-Bromophenyl)-2-hydroxy-2-p-tolylethanone

生成物 1

HCID 203722291-(4-Bromophenyl)-2-p-tolylethane-1,2-dione

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

Cupric sulfate, 90 g. (0.36 mole), is stirred and heated on the steam-bath with 110 ml. of pyridine and 45 ml. of water until complete solution is obtained. 4-Bromo-4'-methylbenzoin, 55 g. (0.18 mole), is added and the mixture is stirred and heated on the steam-bath for 3 hours. During this period, the yellow crystalline product separates. After cooling and dilution with water, the product is collected, washed with water, 1 N hydrochloric acid, and water, and dried; m.p. 132°-135° C. The analytical sample is obtained as yellow needles, m.p. 136°-137° C, after repeated recrystallizations from 95% ethanol.

後処理

  1. temperatureheated on the steam-bath with 110 ml
  2. addition(0.18 mole), is added
  3. stirringthe mixture is stirred
  4. temperatureheated on the steam-bath for 3 hours
  5. waitDuring this period
  6. temperatureAfter cooling
  7. customdilution with water, the product is collected
  8. washwashed with water, 1 N hydrochloric acid, and water
  9. customdried
  10. customThe analytical sample is obtained as yellow needles, m.p. 136°-137° C
  11. customrecrystallizations from 95% ethanol

出典と根拠

ORDレコード
ord-fc2fe1cfc2db40f7be272f90a4563a67
出典データセット
uspto-grants-1978_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04071570

反応ノート

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