Pyridine → Cyclohexyl p-toluenesulfonate

HRID 128557

반응식

HRID 128557 반응식
[CH:1]1([OH:7])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[C:8]1([CH3:18])[CH:13]=[CH:12][C:11]([S:14](Cl)(=[O:16])=[O:15])=[CH:10][CH:9]=1.N1C=CC=CC=1>O>[C:8]1([CH3:18])[CH:13]=[CH:12][C:11]([S:14]([O:7][CH:1]2[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]2)(=[O:16])=[O:15])=[CH:10][CH:9]=1

참가 물질

5

반응물 3

HCID 1049PyridineHCID 73974-Toluenesulfonyl chlorideHCID 7966Cyclohexanol

생성물 1

HCID 13722Cyclohexyl p-toluenesulfonate수율 99.8%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

Cyclohexanol (5.01 g, 50.0 mmol) and p-toluenesulfonyl chloride (10.6 g, 55.6 mmol) were charged into a 100 cc round-bottom flask, and then pyridine (20 ml) was added dropwise thereto under ice-cooling. The mixture was stirred for 8 hours while gradually elevating the temperature to room temperature. After completion of the reaction, cold water (500 ml) was added to the reaction mixture, and the mixture was extracted with ether (100 ml×3). The organic layers were combined, washed successively with 2N hydrochloric acid, water and a saturated aqueous solution of sodium chloride, and dried with anhydrous magnesium sulfate. The drying agent was separated by filtration, and the solvent was distilled off under reduced pressure to obtain substantially pure cyclohexyl p-toluenesulfonate as a white solid (12.7 g, 49.9 mmol, 99% yield).

후처리

  1. temperatureunder ice-cooling
  2. customto room temperature
  3. additionwas added to the reaction mixture
  4. extractionthe mixture was extracted with ether (100 ml×3)
  5. washwashed successively with 2N hydrochloric acid, water
  6. dry with materiala saturated aqueous solution of sodium chloride, and dried with anhydrous magnesium sulfate
  7. customThe drying agent was separated by filtration
  8. distillationthe solvent was distilled off under reduced pressure

출처 및 근거

ORD 기록
ord-6e8538f168ea4c70bab5f5b11227f36d
출처 데이터셋
uspto-grants-1995_11
특허 번호
US05464811

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