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5-Nitro-6-bromo-1h,3h-benzo[de]isochromene → 5-Nitro-1,3-dihydrobenzo[de]isochromene-6-carbonitrile

HRID 217285
ノート
印刷プレビュー

反応式

HRID 217285 の反応式
[N+:1]([C:4]1[C:5](Br)=[C:6]2[CH:15]=[CH:14][CH:13]=[C:12]3[C:7]2=[C:8]([CH:16]=1)[CH2:9][O:10][CH2:11]3)([O-:3])=[O:2].[Cu][C:19]#[N:20]>CN(C=O)C>[N+:1]([C:4]1[C:5]([C:19]#[N:20])=[C:6]2[CH:15]=[CH:14][CH:13]=[C:12]3[C:7]2=[C:8]([CH:16]=1)[CH2:9][O:10][CH2:11]3)([O-:3])=[O:2]
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 578987455-Nitro-6-bromo-1h,3h-benzo[de]isochromeneHCID 178418546HCID 178418546、化合物

生成物 1

HCID 578986665-Nitro-1,3-dihydrobenzo[de]isochromene-6-carbonitrile

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
140 °C

実験手順

5-Nitro-6-bromo-1H,3H-benzo[de]isochromene (23.0 g, 78.2 mmol) was dissolved in anhydrous DMF (500 mL). Then, copper (I) cyanide (10.5 g, 117 mmol) was added to the mixture at room temperature. The mixture was stirred at the internal temperature of 140° C. for 3 hours, and then cooled to 70° C. The resulting insoluble material was separated by filtration. The filtrate was poured into water (1500 mL), and stirred at room temperature for 2 hours. The resulting precipitate was collected by filtration, washed with acetonitrile, and air-dried. The title compound was obtained as yellow solid (15.9 g, 85%).

後処理

  1. temperaturecooled to 70° C
  2. customThe resulting insoluble material was separated by filtration
  3. additionThe filtrate was poured into water (1500 mL)
  4. stirringstirred at room temperature for 2 hours
  5. filtrationThe resulting precipitate was collected by filtration
  6. washwashed with acetonitrile
  7. customair-dried

出典と根拠

ORDレコード
ord-216c678032994032a92faa91f22a2592
出典データセット
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08193351B2

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