Isopropanol → 1-Isopropoxy-1-cyclopentene

HRID 1978248

반응식

HRID 1978248 반응식
[C:1]1(=[O:6])[CH2:5][CH2:4][CH2:3][CH2:2]1.C(OC(C)C)(OC(C)C)O[CH:9]([CH3:11])[CH3:10].C(O)(C)C>O.S([O-])(O)(=O)=O.[Na+]>[CH:9]([O:6][C:1]1[CH2:5][CH2:4][CH2:3][CH:2]=1)([CH3:11])[CH3:10]

참가 물질

5

실험 절차

A mixture of 84.12 grams (1 mol) of cyclopentanone, 195.2 grams (1.03 mol) of triisopropyl orthoformate and 60 grams of isopropanol (1 mol) was stirred in a 500 ml three-neck round bottom flask at room temperature. To this mixture, 3.8 g (0.028 mol) of sodium hydrogensulfate monohydrate was added, and the temperature of the reaction mixture was heated and maintained at 40° C. for about one hour. The progress of the reaction was monitored by GC until the cyclopentanone content was reduced to less than 2%. The isopropanol and isopropyl formate were distilled off under reduced pressure while the temperature of the reaction mixture was increased to a maximum of 65° C. The reaction mixture was cooled to room temperature and the pH value was adjusted to about 7˜8 by adding about 0.2 gram of potassium iso-propoxide. The mixture was then heated under reduced pressure to remove unreacted cyclopentanone and 64 grams (0.51 mol) of 1-isopropoxy-1-cyclopentene was isolated as a clear liquid at a yield of 51%. The purity of the product exceeded 98%.

후처리

  1. temperaturethe temperature of the reaction mixture was heated
  2. temperaturemaintained at 40° C. for about one hour
  3. distillationThe isopropanol and isopropyl formate were distilled off under reduced pressure while the temperature of the reaction mixture
  4. temperaturewas increased to a maximum of 65° C
  5. temperatureThe reaction mixture was cooled to room temperature
  6. additionby adding about 0.2 gram of potassium iso-propoxide
  7. temperatureThe mixture was then heated under reduced pressure
  8. customto remove unreacted cyclopentanone

출처 및 근거

ORD 기록
ord-aa97aff291994268b5fe804748747261
출처 데이터셋
uspto-grants-2001_05
특허 번호
US06235944B1

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