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1-Bromo-2-methylpropane → 5-(2-Methylpropyl)thiophene-2-carboxylic acid

HRID 1094290
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HRID 1094290 반응식
[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[C:6]([OH:8])=[O:7].C1COCC1.[CH2:14](Br)[CH:15]([CH3:17])[CH3:16]>>[CH2:14]([C:5]1[S:1][C:2]([C:6]([OH:8])=[O:7])=[CH:3][CH:4]=1)[CH:15]([CH3:17])[CH3:16]
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참가 물질

4

반응물 3

HCID 65551-Bromo-2-methylpropaneHCID 8028TetrahydrofuranHCID 107002-Thiophenecarboxylic acid

생성물 1

HCID 196226895-(2-Methylpropyl)thiophene-2-carboxylic acid수율 28.2%

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온도
-78 °C

실험 절차

To a solution of 2-thiophene-carboxylic acid (4.16 g, 32.1 mmol) in THF (200 mL) tert. butyllithium (49 mL, 1.7 M solution in pentane, 83.6 mmol) is slowly added at −78° C. The mixture is stirred at −78° C. for 30 min before isobutylbromide (22.7 g, 160.7 mmol) is carefully added. The mixture is stirred at −78° C. for 5 h, then at rt for 16 h. The reaction is quenched by the addition of water (400 mL). The mixture is acidified and extracted with EA. The org. extract is dried over MgSO4, filtered and evaporated. The crude product is purified by MPLC on reverse phase silica gel to give the title compound (1.67 g) as a brownish oil; LC-MS: tR=0.91 min, 1H NMR (CDCl3): δ 0.96 (d, J=6.7 Hz, 6H), 1.94 (hept, J=6.7 Hz, 1H), 2.72 (d, J=7.0 Hz, 2H), 6.80 (d, J=3.8 Hz, 1H), 7.73 (d, J=3.8 Hz, 1H).

후처리

  1. additionis carefully added
  2. waitat rt for 16 h
  3. customThe reaction is quenched by the addition of water (400 mL)
  4. extractionextracted with EA
  5. extractionextract
  6. dry with materialis dried over MgSO4
  7. filtrationfiltered
  8. customevaporated
  9. customThe crude product is purified by MPLC on reverse phase silica gel

출처 및 근거

ORD 기록
ord-5cd44082c49845b890aa93d09c82fe13
출처 데이터셋
uspto-grants-2012_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08133910B2

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