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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Dimethylformamide → Anthranilic acid, N-dimethylaminomethylene-, methyl ester

HRID 1595722
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HRID 1595722 반응식
[C:1]([O:10][CH3:11])(=[O:9])[C:2]1[C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[NH2:4].P(Cl)(Cl)(Cl)=O.[OH-].[Na+].[CH3:19][N:20]([CH3:23])[CH:21]=O>ClCCl>[CH3:19][N:20]([CH:23]=[N:4][C:3]1[CH:5]=[CH:6][CH:7]=[CH:8][C:2]=1[C:1]([O:10][CH3:11])=[O:9])[CH3:21]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 6228DimethylformamideHCID 8635Methyl AnthranilateHCID 14798Sodium HydroxideHCID 24813Phosphorus oxychloride

생성물 1

HCID 13058944Anthranilic acid, N-dimethylaminomethylene-, methyl ester

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a stirred solution of 7.56 g of methyl anthranilate in 50 ml of dimethylformamide at 0° C. was added 5.6 ml of phosphorous oxychloride during 15 m. The mixture was heated at 55 for 45 m, cooled to 0, and diluted with dichloromethane. The mixture was basified at 0° C. by slow addition of cold 1N NaOH to pH 9. The dichloromethane layer was separated, washed with water, dried and concentrated to an oil.

후처리

  1. temperatureThe mixture was heated at 55 for 45 m
  2. temperaturecooled to 0
  3. customThe dichloromethane layer was separated
  4. washwashed with water
  5. customdried
  6. concentrationconcentrated to an oil

출처 및 근거

ORD 기록
ord-e8a60b800d404bacb268e5c3beefec69
출처 데이터셋
uspto-grants-2001_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06288082B1

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