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Ammonia → Ethyl 1-methyl-beta-oxocyclopropanepropanoate

HRID 327378
ノート
印刷プレビュー

反応式

HRID 327378 の反応式
[CH3:1][C:2]1([C:5]([CH:7](C(=O)C)[C:8]([O:10][CH2:11][CH3:12])=[O:9])=[O:6])[CH2:4][CH2:3]1.N>C(O)C>[CH3:1][C:2]1([C:5]([CH2:7][C:8]([O:10][CH2:11][CH3:12])=[O:9])=[O:6])[CH2:3][CH2:4]1
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 222AmmoniaHCID 23363520HCID 23363520、化合物

生成物 1

HCID 10866760Ethyl 1-methyl-beta-oxocyclopropanepropanoate収率 97.5%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

A solution comprising 55 grams of ethyl 2-(1-methylcyclopropanecarbonyl)-3-oxobutanoate and 160 ml of ethanol was stirred at room temperature and 60 ml of a 30% aqueous ammonia solution was added dropwise to this solution over a period of 10 minutes. Subsequently, the mixture was stirred for 1 hour and extracted with 300 ml of ethyl acetate and dilute aqueous hydrochloric acid. After neutralization and washing with water, the organic layer was dried over anhydrous sodium sulfate. The solvent was then removed and 43 grams of ethyl (1-methylcyclopropanecarbonyl)acetate was obtained as an oily material.

後処理

  1. stirringSubsequently, the mixture was stirred for 1 hour
  2. extractionextracted with 300 ml of ethyl acetate and dilute aqueous hydrochloric acid
  3. washAfter neutralization and washing with water
  4. dry with materialthe organic layer was dried over anhydrous sodium sulfate
  5. customThe solvent was then removed

出典と根拠

ORDレコード
ord-7db4c978c0524eaf9adf6835c331852d
出典データセット
uspto-grants-1993_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05273868

反応ノート

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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