2,4-Dinitrobenzenesulfenyl chloride → HCID 20561020、化合物

HRID 1155511

反応式

HRID 1155511 の反応式
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[S:10][CH:11]=[CH:12][C:13]=2[C:14]2[CH:19]=[CH:18][C:17]([O:20][CH3:21])=[CH:16][CH:15]=2)=[CH:5][CH:4]=1.[N+:22]([C:25]1[CH:30]=[C:29]([N+:31]([O-:33])=[O:32])[CH:28]=[CH:27][C:26]=1[S:34]Cl)([O-:24])=[O:23]>FC(F)(F)C(O)=O>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([C:9]2[S:10][C:11]([S:34][C:26]3[CH:27]=[CH:28][C:29]([N+:31]([O-:33])=[O:32])=[CH:30][C:25]=3[N+:22]([O-:24])=[O:23])=[CH:12][C:13]=2[C:14]2[CH:19]=[CH:18][C:17]([O:20][CH3:21])=[CH:16][CH:15]=2)=[CH:7][CH:8]=1

参加物

4

実験手順

A suspension of 2,3-bis(4-methoxyphenyl)thiophene (6.6 g, 22.3 mmoles) and 2,4-dinitrobenzenesulfenyl chloride (5.5 g, 22.3 mmoles) in 55 ml of trifluoroacetic acid was heated at reflux for 15 minutes. The reaction mixture was cooled in ice; the lustrous crystals were collected and washed with cold ether to give the title compound (9.4 g), m.p. 143°-145°

後処理

  1. temperaturewas heated
  2. temperatureat reflux for 15 minutes
  3. temperatureThe reaction mixture was cooled in ice
  4. customthe lustrous crystals were collected
  5. washwashed with cold ether

出典と根拠

ORDレコード
ord-e47269fde309406fb54ae29774fdf931
出典データセット
uspto-grants-1981_11
特許番号
US04302461

関連ノート

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