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Dimethylamine → 1,3-Dimethyl-3-(t-butylperoxy)butyl N,N-dimethylcarbamate

HRID 1447543
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HRID 1447543 반응식
Cl[C:2]([O:4][CH:5]([CH3:16])[CH2:6][C:7]([CH3:15])([O:9][O:10][C:11]([CH3:14])([CH3:13])[CH3:12])[CH3:8])=[O:3].[CH3:17][NH:18][CH3:19]>C(OCC)C>[CH3:17][N:18]([CH3:19])[C:2](=[O:3])[O:4][CH:5]([CH3:16])[CH2:6][C:7]([CH3:15])([O:9][O:10][C:11]([CH3:14])([CH3:13])[CH3:12])[CH3:8]
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참가 물질

4

반응물 2

HCID 674DimethylamineHCID 19612317HCID 19612317, 화합물

생성물 1

HCID 233466071,3-Dimethyl-3-(t-butylperoxy)butyl N,N-dimethylcarbamate

시약·촉매·용매 1

HCID 3283Diethyl Ether용매2회

실험 절차

To a solution of (97%) 1,3-dimethyl-3(t-butylperoxy)butyl chloroformate 5.2 g. (0.02 mole) in diethyl ether, cooled to 0°±1° C. was added a solution of dimethylamine, 1.8 g. (0.04 mole) in diethyl ether over a period of 10 minutes. After the addition was complete the mixture was allowed to stir for two hours while the reaction temperature was allowed to rise to 20°±1° C. The reaction mixture was then filtered to remove the amine hydrochloride and the organic phase washed with 10% aqueous Tartaric acid solution and water to neutrality.

후처리

  1. additionAfter the addition
  2. customto rise to 20°±1° C
  3. filtrationThe reaction mixture was then filtered
  4. customto remove the amine hydrochloride
  5. washthe organic phase washed with 10% aqueous Tartaric acid solution and water to neutrality

출처 및 근거

ORD 기록
ord-ebf7c259fb664c84a1ef853d03cb1438
출처 데이터셋
uspto-grants-1979_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04177204

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