Diketene → benzyl N-(2-acetoacetamidoethyl)carbamate

HRID 1903854노트

반응식

HRID 1903854 반응식
[NH2:1][CH2:2][CH2:3][NH:4][C:5](=[O:14])[O:6][CH2:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1.[CH2:15]=[C:16]1[O:20][C:18](=[O:19])[CH2:17]1>CCOCC>[C:18]([NH:1][CH2:2][CH2:3][NH:4][C:5](=[O:14])[O:6][CH2:7][C:8]1[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=1)(=[O:19])[CH2:17][C:16]([CH3:15])=[O:20]

참가 물질

4

반응물 2

HCID 12661DiketeneHCID 2794257Benzyl N-(2-aminoethyl)carbamate

생성물 1

HCID 20467080benzyl N-(2-acetoacetamidoethyl)carbamate수율 90%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매3회

실험 절차

A solution of benzyl N-(2-aminoethyl)carbamate (54 g, 0.276 mole) in ether (250 ml) and a solution of diketene (25.2 g, 0.30 mole) in ether (250 ml) were added simultaneously, dropwise, to ether (600 ml) while stirring and cooling over a 30 minute period. A white precipitate appeared. The solution was stirred 30 minutes longer, and then filtered. One recrystallization from water gave pure benzyl N-(2-acetoacetamidoethyl)carbamate (m.p.=116°-118° C.) at a yield of 90%.

후처리

  1. temperaturecooling over a 30 minute period
  2. filtrationfiltered
  3. customOne recrystallization from water

출처 및 근거

ORD 기록
ord-1a2ecefccdb3432490efbb1557db8168
출처 데이터셋
uspto-grants-1984_03
특허 번호
US04438278

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