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Diisobutylaluminumhydride → [3-Methyl-4'-(trifluoromethyl)biphenyl-4-yl]methanol

HRID 1669239
ノート
印刷プレビュー

反応式

HRID 1669239 の反応式
C[O:2][C:3]([C:5]1[CH:10]=[CH:9][C:8]([C:11]2[CH:16]=[CH:15][C:14]([C:17]([F:20])([F:19])[F:18])=[CH:13][CH:12]=2)=[CH:7][C:6]=1[CH3:21])=O.[H-].C([Al+]CC(C)C)C(C)C>C(Cl)Cl.C1(C)C=CC=CC=1>[CH3:21][C:6]1[CH:7]=[C:8]([C:11]2[CH:16]=[CH:15][C:14]([C:17]([F:18])([F:19])[F:20])=[CH:13][CH:12]=2)[CH:9]=[CH:10][C:5]=1[CH2:3][OH:2]
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 2

HCID 21225700DiisobutylaluminumhydrideHCID 673420563-Methyl-4'-trifluoromethyl-biphenyl-4-carboxylic acid methyl ester

生成物 1

HCID 22280004[3-Methyl-4'-(trifluoromethyl)biphenyl-4-yl]methanol収率 90%

試薬・触媒・溶媒 2

HCID 1140Toluene溶媒HCID 6344Dichloromethane溶媒

実験手順

A solution of 3-methyl-4′-trifluoromethyl-biphenyl-4-carboxylic acid methyl ester (1.993 g, 6.773 mmol) in CH2Cl2 (34 mL) at 0° C. is treated with 1.0 M diisobutylaluminum hydride in toluene (DIBAL, 14.3 mL) dropwise over 3 min. time and stirred for 3.5 h. The reaction mixture is quenched with MeOH (5.0 mL), treated with 1M tartaric acid (50 mL), and stirred overnight. The organic layer is separated. The aqueous layer is extracted with CH2Cl2 (1×50 mL). Combined organic extracts are dried over MgSO4, filtered, and conc. to provide (3-methyl-4′-trifluoromethyl-biphenyl-4-yl)-methanol (1.616 g, 90%) as a white solid.

後処理

  1. customThe reaction mixture is quenched with MeOH (5.0 mL)
  2. additiontreated with 1M tartaric acid (50 mL)
  3. stirringstirred overnight
  4. customThe organic layer is separated
  5. extractionThe aqueous layer is extracted with CH2Cl2 (1×50 mL)
  6. dry with materialCombined organic extracts are dried over MgSO4
  7. filtrationfiltered

出典と根拠

ORDレコード
ord-b9b42994a2c3425a92ba7ec7fdff5e05
出典データセット
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07989457B2

反応ノート

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