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Formaldehyde → benzyl 2-(N-methyleneamino)-2-methylpropanoate

HRID 377571
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인쇄 미리보기

반응식

HRID 377571 반응식
[CH2:1]=O.[NH2:3][C:4]([CH3:16])([CH3:15])[C:5]([O:7][CH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)=[O:6]>C(OCC)C>[CH2:1]=[N:3][C:4]([CH3:16])([CH3:15])[C:5]([O:7][CH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)=[O:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 712FormaldehydeHCID 11116894Benzyl 2-amino-2-methylpropanoate

생성물 1

HCID 19354575benzyl 2-(N-methyleneamino)-2-methylpropanoate수율 98.9%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매2회

실험 절차

37% Aqueous formaldehyde solution (17.3 g) was added over 10 minutes to a stirred solution of benzyl 2-amino-2-methylpropanoate (28.0 g) in diethyl ether at ambient temperature. The two phase mixture was stirred for 21/2 hours then diluted with diethyl ether and washed with brine. The ethereal solution was dried (magnesium sulphate) and solvent evaporated under reduced pressure to give benzyl 2-(N-methyleneamino)-2-methylpropanoate (29.4 g) in equilibrium with its trimer 1,3,5-tri(1-benzyloxycarbonyl-1-methylethyl)hexahydrotriazine as a colourless oil, IR (liquid film) 2980(m), 1725(vs), 1250(m), 1135(vs).

후처리

  1. washwashed with brine
  2. dry with materialThe ethereal solution was dried (magnesium sulphate) and solvent
  3. customevaporated under reduced pressure

출처 및 근거

ORD 기록
ord-a872f154ffd1449eaf40b5814a199c7a
출처 데이터셋
uspto-grants-2000_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06028032

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