Thiophene → 2-Dodecylthiophene

HRID 1909843

Reaction equation

HRID 1909843 reaction equation
[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]

Participants

5

Conditions

Temperature
-78 °C

Procedure

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%)

Workup

  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

Sources & evidence

ORD record
ord-b1b79fc5324342abbf13dd3266d915ff
Source dataset
uspto-grants-2013_12
Patent number
US08598575B2

Linked notes

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