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2,2-Dimethyl-1,3-dioxane-4,6-dione → 5-((3-Hydroxy-4-methoxyanilino)methylene)-2,2-dimethyl-1,3-dioxane-4,6-dione

HRID 393594
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HRID 393594 반응식
[CH3:1][C:2]1([CH3:10])[O:9][C:7](=[O:8])[CH2:6][C:4](=[O:5])[O:3]1.[OH:11][C:12]1[CH:13]=[C:14]([CH:16]=[CH:17][C:18]=1[O:19][CH3:20])[NH2:15].[CH:21]([O-])([O-])OC>>[OH:11][C:12]1[CH:13]=[C:14]([CH:16]=[CH:17][C:18]=1[O:19][CH3:20])[NH:15][CH:21]=[C:6]1[C:7](=[O:8])[O:9][C:2]([CH3:10])([CH3:1])[O:3][C:4]1=[O:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 162492,2-Dimethyl-1,3-dioxane-4,6-dioneHCID 743145-Amino-2-methoxyphenolHCID 53629101Methylorthoformate

생성물 1

HCID 226465515-((3-Hydroxy-4-methoxyanilino)methylene)-2,2-dimethyl-1,3-dioxane-4,6-dione수율 82%

실험 절차

A solution of Meldrum's acid (32 g, 22.2 mmol)in methyl orthoformate (200 ml) was stirred at 100° C. 3-Hydroxy-4-methoxyaniline (28 g, 20 mmol) was added and the solution was heated at reflux for 15 minutes. After cooling, the mixture was stirred overnight at ambient temperature. The precipitate was collected by filtration, washed with methyl orthoformate followed by ether and dried under vacuum to give 5-((3-hydroxy-4-methoxyanilino)methylene)-2,2-dimethyl-1,3-dioxane-4,6-dione (47.5 g, 82%).

후처리

  1. temperaturethe solution was heated
  2. temperatureat reflux for 15 minutes
  3. temperatureAfter cooling
  4. filtrationThe precipitate was collected by filtration
  5. washwashed with methyl orthoformate
  6. customdried under vacuum

출처 및 근거

ORD 기록
ord-d2dd6c63b71c4d2492a86f0346c5eef9
출처 데이터셋
uspto-grants-2004_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06809097B1

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