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Acetic Acid → HCID 13335396, 화합물

HRID 485125
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HRID 485125 반응식
O[C:2]1([CH3:13])[CH:6]=[CH:5][C:4](=[O:7])[CH:3]1[CH2:8][CH2:9][CH2:10][CH2:11][CH3:12].[C:14]([OH:17])(=[O:16])[CH3:15]>>[CH2:8]([C:3]1[C:4](=[O:7])[CH2:5][CH:6]([O:17][C:14](=[O:16])[CH3:15])[C:2]=1[CH3:13])[CH2:9][CH2:10][CH2:11][CH3:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 176Acetic Acid2회HCID 13137234HCID 13137234, 화합물

생성물 1

HCID 13335396HCID 13335396, 화합물

실험 절차

In the same apparatus as in Example 1, 3-hydroxy-2-n-pentyl-3-methyl-4-cyclopentenone (18.2 g) and acetic acid (55 ml) were charged and heated under reflux for 15 hours with agitation. After the completion of the reaction, acetic acid was evaporated off under reduced pressure. The residue was extracted with toluene (80 ml) and water (50 ml) and treated as in Example 1 to obtain 2-n-pentyl-3-methyl-4-acetoxy-2-cyclopentenone (20.6 g). Yield, 92%. B.P., 125°-135° C./0.2-0.5 mmHg.

후처리

  1. temperatureheated
  2. temperatureunder reflux for 15 hours with agitation
  3. customwas evaporated off under reduced pressure
  4. extractionThe residue was extracted with toluene (80 ml) and water (50 ml)
  5. additiontreated as in Example 1

출처 및 근거

ORD 기록
ord-b325d5c9d338437b99c94e3fe3a683b5
출처 데이터셋
uspto-grants-1985_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04535182

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