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Glycine tert-butyl ester → HCID 178424942, 화합물

HRID 1807024
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HRID 1807024 반응식
[C:1]([O:5][C:6](=[O:9])[CH2:7][NH2:8])([CH3:4])([CH3:3])[CH3:2].[CH3:10][C:11]([C:16]1[O:17][C:18]([CH3:21])=[CH:19][CH:20]=1)([CH3:15])[CH2:12][CH:13]=O>C(Cl)Cl>[C:1]([O:5][C:6](=[O:9])[CH2:7]/[N:8]=[CH:13]/[CH2:12][C:11]([CH3:15])([C:16]1[O:17][C:18]([CH3:21])=[CH:19][CH:20]=1)[CH3:10])([CH3:4])([CH3:3])[CH3:2]
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참가 물질

4

반응물 2

HCID 151417Glycine tert-butyl esterHCID 866404373-Methyl-3-(5-methyl-furan-2-yl)-butyraldehyde

생성물 1

HCID 178424942HCID 178424942, 화합물수율 101.4%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Step F In a manner similar to the method described in Example 1a, glycine tert-butyl ester (0.79 g, 6 mmol) was reacted with 3-methyl-3-(5-methyl-furan-2-yl)-butyraldehyde 1 g, 6 mmol) in CH2Cl2 at room temperature for 5 h to give [3-methyl-3-(5-methyl-furan-2-yl)-but-(E)-ylideneamino]-acetic acid tert-butyl ester as a colorless oil (1.7 g, 100%).

출처 및 근거

ORD 기록
ord-b6bc9f15be8f4373818081574d10629d
출처 데이터셋
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08354444B2

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