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Sodium Propionate → HCID 13335395, 화합물

HRID 485121
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HRID 485121 반응식
C(O[C:5]1([CH3:14])[CH:9]=[CH:8][C:7](=[O:10])[CH:6]1[CH2:11][CH:12]=[CH2:13])(=O)C.[C:15]([O-:19])(=[O:18])[CH2:16][CH3:17].[Na+]>C(O)(=O)CC>[CH2:11]([C:6]1[C:7](=[O:10])[CH2:8][CH:9]([O:19][C:15](=[O:18])[CH2:16][CH3:17])[C:5]=1[CH3:14])[CH:12]=[CH2:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 2723816Sodium PropionateHCID 13335393HCID 13335393, 화합물

생성물 1

HCID 13335395HCID 13335395, 화합물수율 148.5%

시약·촉매·용매 1

HCID 1032Propionic Acid용매2회

실험 절차

In the same apparatus as in Example 1, 3-acetoxy-2-allyl-3-methyl-4-cyclopentenone (19.4 g), propionic acid (70 ml) and sodium propionate (5 g) were charged and agitated at 110° to 120° C. for 6 hours. After the completion of the reaction, propionic acid was evaporated off under reduced pressure. The residue was extracted with toluene (70 ml) and water (40 ml) and treated as in Example 1 to obtain 2-allyl-4-propionyloxy-3-methyl-2-cyclopentenone (16.1 g). Yield, 83%. B.P., 115°-120° C./0.1-0.2 mmHg.

후처리

  1. customwas evaporated off under reduced pressure
  2. extractionThe residue was extracted with toluene (70 ml) and water (40 ml)
  3. additiontreated as in Example 1

출처 및 근거

ORD 기록
ord-a427c184c5cd471eb62c1d508192db79
출처 데이터셋
uspto-grants-1985_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04535182

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