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Bromine → HCID 59629394、化合物

HRID 1395941
ノート
印刷プレビュー

反応式

HRID 1395941 の反応式
[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[C:11]1[CH:12]=[C:13]2[C:22](=[C:23]3[C:28]=1[CH:27]=[CH:26][CH:25]=[CH:24]3)[C:21]1[CH:29]=[CH:30][CH:31]=[CH:32][C:20]=1[C:19]1[C:14]2=[CH:15][CH:16]=[CH:17][CH:18]=1.[Br:33]Br>C(O)(=O)C>[Br:33][C:31]1[CH:30]=[CH:29][C:21]2[C:22]3[C:13]([C:14]4[C:19]([C:20]=2[CH:32]=1)=[CH:18][CH:17]=[CH:16][CH:15]=4)=[CH:12][C:11]([C:2]1[CH:3]=[CH:4][C:5]2[C:10](=[CH:9][CH:8]=[CH:7][CH:6]=2)[CH:1]=1)=[C:28]1[C:23]=3[CH:24]=[CH:25][CH:26]=[CH:27]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 24408BromineHCID 59629392HCID 59629392、化合物

生成物 1

HCID 59629394HCID 59629394、化合物収率 90%

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

反応条件

温度
100 °C

実験手順

4.05 g of 10-(2-naphthyl)benzo[g]chrysene and 400 mL of acetic acid were placed in a flask. 1.92 g of bromine was added, and the resultant was heated with stirring at 100° C. for 8 hours. After cooling to room temperature, the reaction solution was poured to 1 L of ice water. Deposited solids were separated by filtration, and washed with water and then with methanol, and dried. The thus obtained solids were purified by means of silica gel column chromatography, whereby 4.35 g (yield: 90%) of 3-bromo-10-(2-naphthyl)benzo[g]chrysene was obtained.

後処理

  1. temperaturethe resultant was heated
  2. temperatureAfter cooling to room temperature
  3. customDeposited solids were separated by filtration
  4. washwashed with water
  5. dry with materialwith methanol, and dried
  6. customThe thus obtained solids were purified by means of silica gel column chromatography

出典と根拠

ORDレコード
ord-bd37c4f205544db2acadb02fb6b593e5
出典データセット
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08900724B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート