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1-Ethylpiperidine-2,4-dione → 1-Ethyl-3-methoxymethylenepiperidine-2,4-dione

HRID 1252281
ノート
印刷プレビュー

反応式

HRID 1252281 の反応式
[CH:1]([O-])([O-])[O:2][CH3:3].[CH2:6]([N:8]1[CH2:13][CH2:12][C:11](=[O:14])[CH2:10][C:9]1=[O:15])[CH3:7]>C(OC(=O)C)(=O)C>[CH2:6]([N:8]1[CH2:13][CH2:12][C:11](=[O:14])[C:10](=[CH:1][O:2][CH3:3])[C:9]1=[O:15])[CH3:7]
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 137841191-Ethylpiperidine-2,4-dioneHCID 53629101Methylorthoformate

生成物 1

HCID 540921521-Ethyl-3-methoxymethylenepiperidine-2,4-dione収率 25.1%

試薬・触媒・溶媒 1

HCID 7918Acetic Anhydride溶媒

実験手順

11 g of methyl orthoformate and 20 ml of acetic anhydride were added to 8.3 g of 1-ethylpiperidine-2,4-dione, and they were refluxed for 7 hours and then allowed to cool. Excessive methyl orthoformate and acetic anhydride were removed by vacuum distillation. The resulting brown reside was subjected to vacuum distillation (0.5 mmHg, bath temperature of 200° to 250° C.) using a kugelrohr apparatus, whereby 2.7 g of 1-ethyl-3-methoxymethylenepiperidine-2,4-dione was obtained as a crystal with an yield of 25%. This crystal was recrystallized from a mixed solvent consisting of ethyl acetate and hexane to obtain a needle-like crystal of said compound.

後処理

  1. temperaturewere refluxed for 7 hours
  2. temperatureto cool
  3. customExcessive methyl orthoformate and acetic anhydride were removed by vacuum distillation
  4. distillationThe resulting brown reside was subjected to vacuum distillation (0.5 mmHg, bath temperature of 200° to 250° C.)

出典と根拠

ORDレコード
ord-6a5d9c2d500a41b58385f101938adeca
出典データセット
uspto-grants-1988_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04742165

反応ノート

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