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2-(2-Formylethyl)-3-isopropenyl-1-methyl-cyclopent-1-ene → 2-(2-Carboxyethyl)-3-isopropenyl-1-methyl-cyclopent-1-ene

HRID 1834089
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반응식

HRID 1834089 반응식
[CH:1]([CH2:3][CH2:4][C:5]1[CH:9]([C:10]([CH3:12])=[CH2:11])[CH2:8][CH2:7][C:6]=1[CH3:13])=[O:2].CC(C)=[O:16].OS(O)(=O)=O.O=[Cr](=O)=O>CC(C)=O>[C:1]([CH2:3][CH2:4][C:5]1[CH:9]([C:10]([CH3:12])=[CH2:11])[CH2:8][CH2:7][C:6]=1[CH3:13])([OH:16])=[O:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 124807202-(2-Formylethyl)-3-isopropenyl-1-methyl-cyclopent-1-eneHCID 131709961Jones' reagent

생성물 1

HCID 213885332-(2-Carboxyethyl)-3-isopropenyl-1-methyl-cyclopent-1-ene

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

A solution of 25 g of 2-(2-formylethyl)-3-isopropenyl-1-methyl-cyclopent-1-ene in 1200 ml of acetone was treated at -10° C with 55 ml of Jones reagent. The resulting brown mixture was poured on to ice/sodium bicarbonate solution. Ether extraction, washing neutral with sodium bicarbonate solution, saturated sodium chloride solution and water, drying of the extract with magnesium sulphate and removal of the solvent under reduced pressure yielded 20 g (80%) of a weakly yellow oily crude product from which there were obtained by distillation 15 g of pure 2-(2-carboxyethyl)-3-isopropenyl-1-methyl-cyclopent-1-ene; boiling point 0.01 = 102° C; IRfilm : νmax = 3600-2400, 1720, 1645, 1450, 1420, 1380, 1330, 1290, 1220, 1085, 945 and 900 cm-1. The compound has a woody, spicy, weakly sweetish and somewhat musty fragrance.

후처리

  1. extractionEther extraction
  2. washwashing neutral with sodium bicarbonate solution, saturated sodium chloride solution and water
  3. customdrying of the
  4. extractionextract with magnesium sulphate and removal of the solvent under reduced pressure
  5. customyielded 20 g (80%) of a weakly yellow oily crude product from which there

출처 및 근거

ORD 기록
ord-487585eb39a14e6a90c8121d48caff37
출처 데이터셋
uspto-grants-1978_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04068084

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