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Ethyl trifluoroacetate → HCID 117942077, 화합물

HRID 1499107
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HRID 1499107 반응식
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]
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참가 물질

5

반응물 3

HCID 9794Ethyl trifluoroacetateHCID 158289794-bromo-2-methyl-1H-1,3-benzodiazoleHCID 178418339Butyllithium

생성물 1

HCID 117942077HCID 117942077, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
-78 °C

실험 절차

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.

후처리

  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)

출처 및 근거

ORD 기록
ord-256a140ccdec41728bb3dabaf625b3cc
출처 데이터셋
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09199994B2

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