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Thiophene → HCID 12060894、化合物

HRID 1588005
ノート
印刷プレビュー

反応式

HRID 1588005 の反応式
[Br:1][C:2]1[CH:3]=[C:4]([CH:6]=[CH:7][CH:8]=1)N.C(ON=O)CC(C)C.[S:17]1[CH:21]=[CH:20][CH:19]=[CH:18]1>CCOCC>[Br:1][C:2]1[CH:3]=[C:4]([C:18]2[S:17][CH:21]=[CH:20][CH:19]=2)[CH:6]=[CH:7][CH:8]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 8030ThiopheneHCID 8053Isoamyl NitriteHCID 115623-Bromoaniline

生成物 1

HCID 12060894HCID 12060894、化合物収率 34%

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

実験手順

To a stirred solution of m-bromoaniline (34.4 g; 0.2M) in thiophene (200 mL) was added isoamylnitrite (46.86 g; 0.4M) dropwise over a period of 30 mins. at 0° C. The resulting mixture was cautiously warmed to R.T. and heated to reflux for 16 hours. The reaction mixture was cooled, diluted with 400 mL of ether, washed with 3×100 mL of satd. sodium chloride solution, and dried over anhydrous magnesium sulfate. Solvent and excess thiophene were removed. A solution of the residue in 200 mL of ether was filtered through 50 G silica gel bed. Solvent was removed, and the residue was distilled to give 34% of 2-(3'-bromophenyl)thiophene as a yellow liquid boiling at 130°-2°/~0.2 mm. This liquid solidified on standing in the refrigerator.

後処理

  1. customat 0° C
  2. temperatureheated
  3. temperatureto reflux for 16 hours
  4. temperatureThe reaction mixture was cooled
  5. washwashed with 3×100 mL of satd
  6. dry with materialsodium chloride solution, and dried over anhydrous magnesium sulfate
  7. customSolvent and excess thiophene were removed
  8. filtrationA solution of the residue in 200 mL of ether was filtered through 50 G silica gel bed
  9. customSolvent was removed
  10. distillationthe residue was distilled

出典と根拠

ORDレコード
ord-d869d74957a0467b84b53c6e794ee9f7
出典データセット
uspto-grants-1993_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05220011

反応ノート

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