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Phosgene → HCID 12151506, 화합물

HRID 479876
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HRID 479876 반응식
Cl.[CH3:2][NH:3][CH2:4][CH2:5][O:6][C:7](=[O:11])[C:8]([CH3:10])=[CH2:9].[C:12](Cl)([Cl:14])=[O:13]>C(Cl)Cl>[CH3:2][N:3]([CH2:4][CH2:5][O:6][C:7](=[O:11])[C:8]([CH3:10])=[CH2:9])[C:12]([Cl:14])=[O:13]
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참가 물질

4

반응물 2

HCID 6371PhosgeneHCID 22475658HCID 22475658, 화합물

생성물 1

HCID 12151506HCID 12151506, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매

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온도
50 °C

실험 절차

N-Methyl-N-(2-methacryloyloxyethyl)amine hydrochloride (95.0 g, 0.529 mol) produced in Example 1 was suspended in methylene chloride (300 ml) and heated to 50° C. Phosgene (7.85 g, 0.793 mol) was introduced into the resultant suspension over two hours. The resultant reaction mixture was further stirred for one hour, and then the methylene chloride was removed from the mixture to produce N-methyl-N-(2-methacryloyloxyethyl)carbamoyl chloride (106.6 g, almost quantitative yield, purity: 98%) as a colorless transparent liquid. The product was analyzed through gas chromatography (column: silicone SE-30 20% glass column (2 m), injection temperature: 220° C., detection temperature: 230° C.). FIGS. 3 and 4 show the infrared spectrum and NMR spectrum of the product, respectively.

후처리

  1. customThe resultant reaction mixture
  2. customthe methylene chloride was removed from the mixture

출처 및 근거

ORD 기록
ord-127672a56e5f4f6dae5f858ba2c96500
출처 데이터셋
uspto-grants-2003_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06646156B2

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