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2-Methylindole → 2-(1H-indol-2-ylmethyl)-1,1,1-trifluoro-4-(4-fluorophenyl)-4-methylpentan-2-ol

HRID 1510879
ノート
印刷プレビュー

反応式

HRID 1510879 の反応式
[CH3:1][C:2]1[NH:3][C:4]2[C:9]([CH:10]=1)=[CH:8][CH:7]=[CH:6][CH:5]=2.C([Li])CCC.CC(C)([O-])C.[K+].[F:22][C:23]([F:38])([F:37])[C:24](=[O:36])[CH2:25][C:26]([C:29]1[CH:34]=[CH:33][C:32]([F:35])=[CH:31][CH:30]=1)([CH3:28])[CH3:27]>C(OCC)C>[NH:3]1[C:4]2[C:9](=[CH:8][CH:7]=[CH:6][CH:5]=2)[CH:10]=[C:2]1[CH2:1][C:24]([OH:36])([CH2:25][C:26]([C:29]1[CH:30]=[CH:31][C:32]([F:35])=[CH:33][CH:34]=1)([CH3:28])[CH3:27])[C:23]([F:22])([F:38])[F:37]
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 72242-MethylindoleHCID 220326931,1,1-Trifluoro-4-(4-fluorophenyl)-4-methylpentan-2-oneHCID 23665647Potassium tert-butoxideHCID 178418339Butyllithium

生成物 1

HCID 101264152-(1H-indol-2-ylmethyl)-1,1,1-trifluoro-4-(4-fluorophenyl)-4-methylpentan-2-ol収率 26.2%

試薬・触媒・溶媒 1

HCID 3283
Diethyl Ether
溶媒
2 回

実験手順

To a diethyl ether solution of 53 mg of 2-methylindole was added 3 equivalents of n-butyl lithium followed by 90 mg of potassium tert-butoxide (t-BuOK) (solid) at room temperature. The mixture was allowed to stir for 30 minutes. 1,1,1-Trifluoro-4-(4-fluorophenyl)-4-methylpentan-2-one (100 mg) in diethyl ether was then added to the above mixture. The reaction was stirred at room for 1 hour. The reaction was quenched with saturated aqueous ammonium chloride, and extracted three times with EtOAc. The combined organic layers were washed with water, brine, dried over magnesium sulfate, filtered, and concentrated in vacuo. The residue was purified by column chromatography to yield 40 mg of the title compound as a foam. Resolution to the (+)- and (−) enantiomers was accomplished by chiral HPLC on a CHIRALCEL® OD™ column, eluting with 10% isopropanol-hexanes.

後処理

  1. stirringThe reaction was stirred at room for 1 hour
  2. customThe reaction was quenched with saturated aqueous ammonium chloride
  3. extractionextracted three times with EtOAc
  4. washThe combined organic layers were washed with water, brine
  5. dry with materialdried over magnesium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. customThe residue was purified by column chromatography

出典と根拠

ORDレコード
ord-c6a3ac5ebb86443591e2071343e048a6
出典データセット
uspto-grants-2012_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08212040B2

反応ノート

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