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

Iodoethane → Methyl 1-ethyl-2-oxocyclopentane-1-carboxylate

HRID 132766
ノート
印刷プレビュー

反応式

HRID 132766 の反応式
[O:1]=[C:2]1[CH2:6][CH2:5][CH2:4][CH:3]1[C:7]([O:9][CH3:10])=[O:8].C(=O)([O-])[O-].[K+].[K+].[CH2:17](I)[CH3:18]>CC(C)=O>[CH2:17]([C:3]1([C:7]([O:9][CH3:10])=[O:8])[CH2:4][CH2:5][CH2:6][C:2]1=[O:1])[CH3:18]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 6340IodoethaneHCID 11430Potassium CarbonateHCID 66328Cyclopentanecarboxylic acid, 2-oxo-, methyl ester

生成物 1

HCID 12586400Methyl 1-ethyl-2-oxocyclopentane-1-carboxylate収率 101.6%

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

Under vigorously agitation, 14.8 g of methyl 2-oxocyclopentane carboxylate was added to 41.9 g of fine powdery anhydrous potassium carbonate, and after stirring for several minutes, to the mixture was added 100 ml of acetone. The reaction mixture was further stirred for 15 to 30 minutes at room temperature, then thereto was dropwise added 31.2 g of ethyl iodide. Upon the completion of the addition, the reaction mixture was heated for reflux for 2 hours. The solvent was removed under reduced pressure, and solid residue was washed with diethyl ether. The washing liquor was collected and washed with water. After removing the solvent, 18.0 g of pale yellow liquid was obtained, The liquid was distilled under reduced pressure, and 15.9 g of colorless liquid as a distillate cut of 122-124° C./25 mmHg was collected. Yield: 93.5%.

後処理

  1. stirringThe reaction mixture was further stirred for 15 to 30 minutes at room temperature
  2. additionUpon the completion of the addition
  3. temperaturethe reaction mixture was heated
  4. temperaturefor reflux for 2 hours
  5. customThe solvent was removed under reduced pressure, and solid residue
  6. washwas washed with diethyl ether
  7. customThe washing liquor was collected
  8. washwashed with water
  9. customAfter removing the solvent

出典と根拠

ORDレコード
ord-4a68fffe941849c191da0e1b2fae572d
出典データセット
uspto-grants-2008_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07388103B2

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