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Diethyl Malonate → 1,3-Dihydroindene-2,2-dicarboxylic acid

HRID 356881
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HRID 356881 반응식
[Na].[C:2]([O:10]CC)(=[O:9])[CH2:3][C:4]([O:6]CC)=[O:5].Br[CH:14](Br)[C:15]1[C:16]([CH3:21])=[CH:17][CH:18]=[CH:19][CH:20]=1>C(O)C.C(OCC)C>[CH2:21]1[C:16]2[C:15](=[CH:20][CH:19]=[CH:18][CH:17]=2)[CH2:14][C:3]1([C:4]([OH:6])=[O:5])[C:2]([OH:10])=[O:9]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 7761Diethyl MalonateHCID 6390401-(Dibromomethyl)-2-methylbenzeneHCID 5360545Sodium

생성물 1

HCID 2519571,3-Dihydroindene-2,2-dicarboxylic acid

시약·촉매·용매 2

HCID 702Ethanol용매HCID 3283Diethyl Ether용매2회

실험 절차

Sodium (3.7 g) was dissolved in 80 ml of ethyl alcohol, followed by the addition of 150 ml of diethyl ether. Diethyl malonate (12.5 ml) was added followed by 20 g of α, α-dibromo-o-xylene in 150 ml of diethyl ether with overhead stirring. The reaction was heated to reflux for 5 hours. The reaction was cooled, filtered, and the solvent was removed under vacuum. The residue was treated with a potassium hydroxide solution (20 g in 125 ml of water) and heated to reflux for 15 hours. The reaction was then cooled and rinsed with 200 ml of diethyl ether. The aqueous phase was acidified with 30% hydrochloric acid. The precipitate was collected and dried under vacuum over Drieruite for 5 hours to yield 8.86 g of indan-2,2-dicarboxylic acid.

후처리

  1. temperatureThe reaction was heated
  2. temperatureto reflux for 5 hours
  3. temperatureThe reaction was cooled
  4. filtrationfiltered
  5. customthe solvent was removed under vacuum
  6. additionThe residue was treated with a potassium hydroxide solution (20 g in 125 ml of water)
  7. temperatureheated
  8. temperatureto reflux for 15 hours
  9. temperatureThe reaction was then cooled
  10. washrinsed with 200 ml of diethyl ether
  11. customThe precipitate was collected
  12. customdried under vacuum over Drieruite for 5 hours

출처 및 근거

ORD 기록
ord-0d01fc71497f4be98785cde4fd3f67e2
출처 데이터셋
uspto-grants-1998_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05840729

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