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Ethyl trifluoroacetate → HCID 117942077、化合物

HRID 1499107
ノート
印刷プレビュー

反応式

HRID 1499107 の反応式
Br[C:2]1[C:10]2[N:9]=[C:8]([CH3:11])[NH:7][C:6]=2[CH:5]=[CH:4][CH:3]=1.C([Li])CCC.C([O:19][C:20](=O)[C:21]([F:24])([F:23])[F:22])C>C1COCC1>[F:22][C:21]([F:24])([F:23])[C:20]([C:2]1[C:10]2[N:9]=[C:8]([CH3:11])[NH:7][C:6]=2[CH:5]=[CH:4][CH:3]=1)=[O:19]
参加物反応条件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 9794Ethyl trifluoroacetateHCID 158289794-bromo-2-methyl-1H-1,3-benzodiazoleHCID 178418339Butyllithium

生成物 1

HCID 117942077HCID 117942077、化合物

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
-78 °C

実験手順

4-Bromo-2-methyl-1H-benzimidazole (500 mg, 2.37 mmol) was dissolved in THF (8 mL) and cooled to −78° C. n-Butyllithium (2.3 mL, 2.5 M in hexanes, 5.7 mmol) was added dropwise and the reaction was stirred at −78° C. for 30 min. Trifluoroacetic acid ethyl ester (339 μL, 2.8 mmol) was added and the reaction was stirred at 0° C. for 1 h. The reaction was quenched with HCl (2 N, 4 mL), then extracted with water and EtOAc, washed with brine, dried over Na2SO4, filtered, and concentrated in vacuo. Purification by normal phase silica gel column chromatography (CH2Cl2/MeOH/NH4OH) provided 2,2,2-trifluoro-1-(2-methyl-1H-benzoimidazol-4-yl)-ethanone.

後処理

  1. additionwas added dropwise
  2. stirringthe reaction was stirred at 0° C. for 1 h
  3. customThe reaction was quenched with HCl (2 N, 4 mL)
  4. extractionextracted with water and EtOAc
  5. washwashed with brine
  6. dry with materialdried over Na2SO4
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo
  9. customPurification by normal phase silica gel column chromatography (CH2Cl2/MeOH/NH4OH)

出典と根拠

ORDレコード
ord-256a140ccdec41728bb3dabaf625b3cc
出典データセット
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09199994B2

反応ノート

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