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1,2-Dimethoxyethane → 2,2-Bis-(4-fluoro-phenyl)-4-hydroxy-butyronitrile

HRID 1272391
ノート
印刷プレビュー

反応式

HRID 1272391 の反応式
COCCOC.[BH4-].[Na+].[Li+].[Cl-].C([O:13][C:14](=O)[CH2:15][C:16]([C:31]#[N:32])([C:24]1[CH:29]=[CH:28][C:27]([F:30])=[CH:26][CH:25]=1)[C:17]1[CH:22]=[CH:21][C:20]([F:23])=[CH:19][CH:18]=1)C>O>[F:23][C:20]1[CH:19]=[CH:18][C:17]([C:16]([C:24]2[CH:25]=[CH:26][C:27]([F:30])=[CH:28][CH:29]=2)([CH2:15][CH2:14][OH:13])[C:31]#[N:32])=[CH:22][CH:21]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 80711,2-DimethoxyethaneHCID 433294Lithium Chloride2 回HCID 4311764Sodium borohydride2 回HCID 58849420HCID 58849420、化合物

生成物 1

HCID 184570632,2-Bis-(4-fluoro-phenyl)-4-hydroxy-butyronitrile

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

Ethylene glycol dimethyl ether (10 ml) was treated with sodium borohydride (142 mg) and LiCl (228 mg) and the mixture stirred for 30 min. 3-Cyano-3,3-bis-(4-fluoro-phenyl)-propionic acid ethyl ester (847 mg) was added and the mixture stirred for 6 hrs, before more sodium borohydride (36 mg) and LiCl (57 mg) were added and stirring continued overnight. The mixture was poured into water and extracted (3×) with ethyl ether. The combined organic extracts were dried over Na2SO4. Filtration, concentration and flash chromatography of the residue afforded the title compound (41%; Isolated as an oil).

後処理

  1. additionwere added
  2. stirringstirring continued overnight
  3. extractionextracted (3×) with ethyl ether
  4. dry with materialThe combined organic extracts were dried over Na2SO4
  5. filtrationFiltration, concentration and flash chromatography of the residue

出典と根拠

ORDレコード
ord-b38f30a0962242278ceb6717fe0307df
出典データセット
uspto-grants-2007_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07208527B2

反応ノート

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