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Lithium (trimethylsilyl)acetylide → 2-((R)-3-hydroxy-1,1-dimethyl-3-trifluoromethyl-6-trimethylsilanylhex-5-ynyl)benzamide

HRID 2387327
ノート
印刷プレビュー

反応式

HRID 2387327 の反応式
[CH3:1][C:2]([C:12]1[CH:20]=[CH:19][CH:18]=[CH:17][C:13]=1[C:14]([NH2:16])=[O:15])([CH3:11])[CH2:3][C@:4]1([C:7]([F:10])([F:9])[F:8])[CH2:6][O:5]1.C([Mg]CCCC)CCC.[Li+].[CH3:31][Si:32]([C:35]#[C-:36])([CH3:34])[CH3:33]>COCCOC>[OH:5][C@@:4]([C:7]([F:8])([F:9])[F:10])([CH2:6][C:36]#[C:35][Si:32]([CH3:34])([CH3:33])[CH3:31])[CH2:3][C:2]([C:12]1[CH:20]=[CH:19][CH:18]=[CH:17][C:13]=1[C:14]([NH2:16])=[O:15])([CH3:11])[CH3:1]
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 3

HCID 3431600Lithium (trimethylsilyl)acetylideHCID 580261682-[1,1-dimethyl-2-((R)-2-trifluoromethyloxiranyl)ethyl]benzamideHCID 178448196HCID 178448196、化合物

生成物 1

HCID 580261722-((R)-3-hydroxy-1,1-dimethyl-3-trifluoromethyl-6-trimethylsilanylhex-5-ynyl)benzamide

試薬・触媒・溶媒 1

HCID 80711,2-Dimethoxyethane溶媒

実験手順

To a stirred, ice-cooled, solution of (trimethylsilyl)acetylene (72.6 mL, 514 mmol) in 500 mL of ethylene glycol dimethyl ether was added n-butyllithium (185 mL of 2.5 M solution in hexanes, 462 mmol). The reaction mixture, which turned from a colorless to a yellowish solution, was stirred for 50 minutes to give a solution of 462 mmol of lithium (trimethylsilyl)acetylide. A stirred solution of 2-[1,1-dimethyl-2-((R)-2-trifluoromethyloxiranyl)ethyl]benzamide (26.5 g, 92.3 mmol) in ethylene glycol dimethyl ether (250 mL) was cooled to −30° C. Dibutylmagnesium (50.8 mL of 1 M solution in heptane, 50.8 mmol) was added and the mixture stirred for 45 minutes. The above solution of lithium (trimethylsilyl)acetylide was added and the stirring continued at −20° C. After 5 minutes, cooling bath was removed and the reaction mixture was stirred for 3 hours and 15 minutes. The reaction was quenched with 600 mL of saturated ammonium chloride solution and extracted with four 250 mL portions of ethyl acetate. The combined organic extracts were washed with two 250 mL portions of brine, dried over anhydrous sodium sulfate, and the solvent removed in vacuo to give 2-((R)-3-hydroxy-1,1-dimethyl-3-trifluoromethyl-6-trimethylsilanylhex-5-ynyl)benzamide as brownish oil (27 g).

後処理

  1. customcontinued at −20° C
  2. waitAfter 5 minutes
  3. temperaturecooling bath
  4. customwas removed
  5. stirringthe reaction mixture was stirred for 3 hours and 15 minutes
  6. customThe reaction was quenched with 600 mL of saturated ammonium chloride solution
  7. extractionextracted with four 250 mL portions of ethyl acetate
  8. washThe combined organic extracts were washed with two 250 mL portions of brine
  9. dry with materialdried over anhydrous sodium sulfate
  10. customthe solvent removed in vacuo

出典と根拠

ORDレコード
ord-64d9e1e969e64d82abdd707f6365903a
出典データセット
uspto-grants-2012_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08268859B2

反応ノート

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