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

Methyl 4-pyridin-3-ylbenzoate → [4-(Pyridin-3-yl)phenyl]methanol

HRID 1274256
ノート
印刷プレビュー

反応式

HRID 1274256 の反応式
C[O:2][C:3](=O)[C:4]1[CH:9]=[CH:8][C:7]([C:10]2[CH:11]=[N:12][CH:13]=[CH:14][CH:15]=2)=[CH:6][CH:5]=1.[H-].C([Al+]CC(C)C)C(C)C>C(Cl)Cl>[N:12]1[CH:13]=[CH:14][CH:15]=[C:10]([C:7]2[CH:8]=[CH:9][C:4]([CH2:3][OH:2])=[CH:5][CH:6]=2)[CH:11]=1
参加物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 4133187Methyl 4-pyridin-3-ylbenzoateHCID 21225700Diisobutylaluminumhydride

生成物 1

HCID 1515243[4-(Pyridin-3-yl)phenyl]methanol収率 96.6%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

To a solution of 4-pyridin-3-yl-benzoic acid methyl ester (124 mg in 5.0 mL dry methylene chloride) at -78° C. was added 1.46 mL of a 1M solution of diisobutylaluminum hydride in methylene chloride and the mixture stirred at low temperature. After 2 hours, the reaction was quenched by the addition of acetone, warmed to room temperature and stirred for 20 minutes with 1.5 mL of a 1M solution of tartaric acid. At this time the mixture was extracted with methylene chloride and the combined organics dried over sodium sulfate. Purification of the concentrate by flash chromatography on silica gel (ethyl acetate:hexane, 1:1; then methylene chloride:methanol, 95:5) gave the title compound (104 mg).

後処理

  1. customthe reaction was quenched by the addition of acetone
  2. stirringstirred for 20 minutes with 1.5 mL of a 1M solution of tartaric acid
  3. extractionAt this time the mixture was extracted with methylene chloride
  4. dry with materialthe combined organics dried over sodium sulfate
  5. customPurification of the
  6. concentrationconcentrate by flash chromatography on silica gel (ethyl acetate

出典と根拠

ORDレコード
ord-189f404431bc4b708fbdd0203a0f79f2
出典データセット
uspto-grants-2000_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06156772

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート