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

HRID 1252281
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HRID 1252281 반응식
[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]
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참가 물질

4

반응물 2

HCID 137841191-Ethylpiperidine-2,4-dioneHCID 53629101Methylorthoformate

생성물 1

HCID 540921521-Ethyl-3-methoxymethylenepiperidine-2,4-dione수율 25.1%

시약·촉매·용매 1

HCID 7918Acetic Anhydride용매

실험 절차

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.

후처리

  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.)

출처 및 근거

ORD 기록
ord-6a5d9c2d500a41b58385f101938adeca
출처 데이터셋
uspto-grants-1988_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04742165

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