Dimethyl malonate → Dimethyl (3-oxo-2-pentylcyclopentyl)malonate

HRID 1793218

반응식

HRID 1793218 반응식
[CH2:1]([C:6]1[C:7](=[O:11])[CH2:8][CH2:9][CH:10]=1)[CH2:2][CH2:3][CH2:4][CH3:5].[C:12]([O:19][CH3:20])(=[O:18])[CH2:13][C:14]([O:16][CH3:17])=[O:15].C[O-].[Na+]>>[CH2:1]([CH:6]1[C:7](=[O:11])[CH2:8][CH2:9][CH:10]1[CH:13]([C:12]([O:19][CH3:20])=[O:18])[C:14]([O:16][CH3:17])=[O:15])[CH2:2][CH2:3][CH2:4][CH3:5]

참가 물질

4

반응물 3

HCID 7943Dimethyl malonateHCID 1175492-Cyclopenten-1-one, 2-pentyl-HCID 10942334Sodium Methoxide

생성물 1

HCID 103546Dimethyl (3-oxo-2-pentylcyclopentyl)malonate수율 93.8%

반응 조건

온도
0 °C

실험 절차

The reaction product was refined to obtain 95 g (0.6 mol) of 2-pentyl-2-cyclopentenone. Moreover, 95 g (0.6 mol) of 2-pentyl-2-cyclopentenone was dropped to a solution, prepared by dissolving 118 g (0.9 mol) of dimethyl malonate in 38 g of methanol anhydride in a nitrogen atmosphere, cooling the mixture to 0° C. and adding 6.5 g (0.036 mol) of sodium methoxide (30% methanol solution), at 0° C. over 2 hours. After the addition was finished, unreacted dimethyl malonate was vacuum-distilled to obtain 160 g of dimethyl 2-pentyl-3-oxo-cyclopentylmalonate.

후처리

  1. customprepared
  2. additionAfter the addition
  3. distillationunreacted dimethyl malonate was vacuum-distilled

출처 및 근거

ORD 기록
ord-f9af51249e6348399a70185518c0bc2d
출처 데이터셋
uspto-grants-2006_07
특허 번호
US07078559B2

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