ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Potassium Hydroxide → 3-Ethylcyclobutane-1,1-dicarboxylic acid

HRID 27293
ノート
印刷プレビュー

反応式

HRID 27293 の反応式
[CH2:1]([CH:3]1[CH2:6][C:5]([C:12]([O:14]CC)=[O:13])([C:7]([O:9]CC)=[O:8])[CH2:4]1)[CH3:2].[OH-].[K+]>C(O)C>[CH2:1]([CH:3]1[CH2:4][C:5]([C:12]([OH:14])=[O:13])([C:7]([OH:9])=[O:8])[CH2:6]1)[CH3:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 14797Potassium HydroxideHCID 20041463Diethyl 3-ethylcyclobutane-1,1-dicarboxylate

生成物 1

HCID 200414433-Ethylcyclobutane-1,1-dicarboxylic acid収率 84.3%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒2 回

実験手順

A solution of 7.0 g (0.031 mole) of 3-ethyl-1,1-dicarbethoxycyclobutane (prepared in 1C) dissolved in 7 ml of absolute ethanol was prepared. To this solution there was added 6.87 g (0.123 mole) of potassium hydroxide dissolved in 76 ml of absolute ethanol and the mixture was heated to reflux with stirring for 1.5 hr. The mixture was then filtered and the filter cake was washed with 10 ml of absolute ethanol and 75 ml of ether. The resulting filter cake was dissolved in 30 ml of ice water and acidified with 36 ml of 50% aqueous sulfuric acid. The resulting mixture was cooled, filtered and dried to yield 4.5 g of the title compound having the following physical characteristics:

後処理

  1. customwas prepared
  2. temperaturethe mixture was heated
  3. temperatureto reflux
  4. filtrationThe mixture was then filtered
  5. washthe filter cake was washed with 10 ml of absolute ethanol and 75 ml of ether
  6. filtrationThe resulting filter cake
  7. dissolutionwas dissolved in 30 ml of ice water
  8. temperatureThe resulting mixture was cooled
  9. filtrationfiltered
  10. customdried

出典と根拠

ORDレコード
ord-07d36e2b18be4e8486728267d48f49c7
出典データセット
uspto-grants-1980_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04220795

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート