Thiophene → 2-Dodecylthiophene

HRID 1909843

반응식

HRID 1909843 반응식
[S:1]1[CH:5]=[CH:4][CH:3]=[CH:2]1.[Li]CCCC.[CH2:11](Br)[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH3:22]>C1COCC1>[CH2:22]([C:2]1[S:1][CH:5]=[CH:4][CH:3]=1)[CH2:21][CH2:20][CH2:19][CH2:18][CH2:17][CH2:16][CH2:15][CH2:14][CH2:13][CH2:12][CH3:11]

참가 물질

5

반응 조건

온도
-78 °C

실험 절차

A solution of thiophene (14.3 g, 0.17 mol) in dry THF (150 mL) was cooled to −78° C. under nitrogen. A solution of n-BuLi (38.0 mL, 2.5 M, 95.0 mmol) was then added dropwise over a course of 40 minutes. After addition, the reaction mixture was stirred at −78° C. for additional 2 hours, before a solution of n-C12H25Br (16.9 g, 67.8 mmol) in dry THF (25 mL) was added slowly. This mixture was stirred at −78° C. for 1 hour, and then allowed to warm to room temperature slowly and stirred at room temperature overnight. The reaction was quenched by water (20 mL) and the mixture was poured into water (400 mL), and the resulting mixture was extracted with ether (400 mL). The organic layer was washed with water and brine, dried over MgSO4, and concentrated on a rotary evaporator. The residue was subjected to column chromatography on silica gel with hexane as eluent, leading to a colorless oil as the product. (8.68 g, 50.7%)

후처리

  1. additionAfter addition
  2. additionwas added slowly
  3. temperatureto warm to room temperature slowly
  4. stirringstirred at room temperature overnight
  5. customThe reaction was quenched by water (20 mL)
  6. additionthe mixture was poured into water (400 mL)
  7. extractionthe resulting mixture was extracted with ether (400 mL)
  8. washThe organic layer was washed with water and brine
  9. dry with materialdried over MgSO4
  10. concentrationconcentrated on a rotary evaporator

출처 및 근거

ORD 기록
ord-b1b79fc5324342abbf13dd3266d915ff
출처 데이터셋
uspto-grants-2013_12
특허 번호
US08598575B2

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