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HCID 14923755、化合物 → 2,7-Dimethoxy-9H-carbazole

HRID 1614998
ノート
印刷プレビュー

反応式

HRID 1614998 の反応式
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[CH:14]=[CH:13][C:12]([O:15][CH3:16])=[CH:11][CH:10]=2)=[C:5]([N+:17]([O-])=O)[CH:4]=1>P(OCC)(OCC)OCC>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]2[C:9]3[C:14](=[CH:13][C:12]([O:15][CH3:16])=[CH:11][CH:10]=3)[NH:17][C:5]=2[CH:4]=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

3

反応物 1

HCID 14923755HCID 14923755、化合物

生成物 1

HCID 123393992,7-Dimethoxy-9H-carbazole

試薬・触媒・溶媒 1

HCID 31215Triethyl phosphite溶媒

反応条件

温度
90 °C

実験手順

The reaction was carried out in a vial. The crude biphenyl 10h (6.0 g) was dissolved in P(OEt)3 (36 mL). The vial was flushed with argon. The reaction mixture was heated to 90° C., kept at this temperature overnight, and cooled. As a result the carbazole precipitated. Et2O/CH2Cl2 mixture was added. The precipitate was filtered off and washed with CH2Cl2. The filtrate was evaporated. P(OEt)3 was added again, and the mixture was left for cyclization for 24 h. These operations were repeated until the precipitate formation ceased, and TLC indicated that the starting biphenyl disappeared. In total 2.9 g of the carbazole was obtained (65% calculated for two steps.)

後処理

  1. customThe vial was flushed with argon
  2. customkept at this temperature overnight
  3. temperaturecooled

出典と根拠

ORDレコード
ord-8a367792293a49bdbf636b3d2b756b21
出典データセット
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08765738B2

反応ノート

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