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

HRID 356881
ノート
印刷プレビュー

反応式

HRID 356881 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

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

生成物 1

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

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 3283Diethyl Ether溶媒2 回

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-0d01fc71497f4be98785cde4fd3f67e2
出典データセット
uspto-grants-1998_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05840729

反応ノート

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