ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Dimethylformamide → 3-Phenylbenzo[b]thiophene-2-carbaldehyde

HRID 1906757
ノート
印刷プレビュー

反応式

HRID 1906757 の反応式
C([Li])CCC.[C:6]1([C:12]2[C:13]3[CH:20]=[CH:19][CH:18]=[CH:17][C:14]=3[S:15][CH:16]=2)[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1.CN(C)[CH:23]=[O:24]>O1CCCC1>[C:6]1([C:12]2[C:13]3[CH:20]=[CH:19][CH:18]=[CH:17][C:14]=3[S:15][C:16]=2[CH:23]=[O:24])[CH:7]=[CH:8][CH:9]=[CH:10][CH:11]=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

5

反応物 3

HCID 6228DimethylformamideHCID 6108813-PhenylbenzothiopheneHCID 178418339Butyllithium

生成物 1

HCID 105141003-Phenylbenzo[b]thiophene-2-carbaldehyde

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
-70 °C

実験手順

Butyllithium (62.5 ml of 1.6M solution in hexane, 0.1 mole) was added dropwise to a stirred solution of 3-phenylbenzo[b]thiophene (21.0 g, 0.1 mole) in tetrahydrofuran (150 ml) at -70° C. The solution was stirred at -70° C. for 30 minutes and dimethylformamide (10 ml, 0.13 mole) was added. The resulting mixture was stirred at -70° C. for 30 minutes and then allowed to warm to ambient temperature. After a further hour the reaction was quenched by the addition of dilute hydrochloric acid (100 ml, 2M) and the tetrahydrofuran removed under reduced pressure. The resulting oil was extracted into diethyl ether, the ethereal extract washed with water, dried over potassium carbonate and concentrated.

後処理

  1. stirringThe resulting mixture was stirred at -70° C. for 30 minutes
  2. temperatureto warm to ambient temperature
  3. customAfter a further hour the reaction was quenched by the addition of dilute hydrochloric acid (100 ml, 2M)
  4. customthe tetrahydrofuran removed under reduced pressure
  5. extractionThe resulting oil was extracted into diethyl ether
  6. extractionthe ethereal extract
  7. washwashed with water
  8. dry with materialdried over potassium carbonate
  9. concentrationconcentrated

出典と根拠

ORDレコード
ord-6ab892673fc045028a5497921f9c43ee
出典データセット
uspto-grants-1987_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04654352

反応ノート

読み込み中…

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