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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Water → Ethyl [(2-methylacryloyl)amino](oxo)acetate

HRID 1032076
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HRID 1032076 반응식
[C:1](Cl)([C:3]([O:5][CH2:6][CH3:7])=[O:4])=[O:2].[C:9]([NH2:14])(=[O:13])[C:10]([CH3:12])=[CH2:11].O>C(Cl)(Cl)Cl>[C:1]([NH:14][C:9](=[O:13])[C:10]([CH3:12])=[CH2:11])([C:3]([O:5][CH2:6][CH3:7])=[O:4])=[O:2]
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참가 물질

5

반응물 3

HCID 962WaterHCID 6595MethacrylamideHCID 20884Ethoxalyl chloride

생성물 1

HCID 14298183Ethyl [(2-methylacryloyl)amino](oxo)acetate수율 28.8%

시약·촉매·용매 1

HCID 6212Chloroform용매2회

실험 절차

Into the same reaction vessel as used in Example 1, ethoxalyl chloride (12.3 g; 0.09 mol) was charged, and the reaction vessel was cooled in an ice bath. A solution of methacrylamide (20.3 g; 0.24 mol) in chloroform (90.0 ml) was dropwise added thereto in 30 minutes, followed by stirring at room temperature for 3 days. The reaction mixture was shaken with chloroform (500 ml) and water (500 ml), and the chloroform layer was separated and dried over anhydrous magnesium sulfate, followed by removal of chloroform. Hydroquinone (0.01 g) was added thereto, and distillation under reduced pressure was carried out to give N-ethoxalylmethacrylamide (4.8 g). Yield, 29%.

후처리

  1. additionwas charged
  2. temperaturethe reaction vessel was cooled in an ice bath
  3. customthe chloroform layer was separated
  4. dry with materialdried over anhydrous magnesium sulfate
  5. customfollowed by removal of chloroform
  6. additionHydroquinone (0.01 g) was added
  7. distillationdistillation under reduced pressure

출처 및 근거

ORD 기록
ord-bf268c957c4d48caa7a2f735b3cec38e
출처 데이터셋
uspto-grants-1990_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04956491

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