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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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1-tert-Butyl 3-ethyl 3-cyanoazetidine-1,3-dicarboxylate → 1-Tert-butyl 3-methyl 3-(aminomethyl)azetidine-1,3-dicarboxylate

HRID 1175153
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HRID 1175153 반응식
[CH2:1]([O:3][C:4]([C:6]1([C:17]#[N:18])[CH2:9][N:8]([C:10]([O:12][C:13]([CH3:16])([CH3:15])[CH3:14])=[O:11])[CH2:7]1)=[O:5])C.[H][H]>CO.[Ni]>[CH3:1][O:3][C:4]([C:6]1([CH2:17][NH2:18])[CH2:9][N:8]([C:10]([O:12][C:13]([CH3:14])([CH3:16])[CH3:15])=[O:11])[CH2:7]1)=[O:5]
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참가 물질

5

반응물 2

HCID 595585001-tert-Butyl 3-ethyl 3-cyanoazetidine-1,3-dicarboxylateHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 595583501-Tert-butyl 3-methyl 3-(aminomethyl)azetidine-1,3-dicarboxylate

시약·촉매·용매 2

HCID 935Nickel촉매HCID 887Methanol용매

실험 절차

3-Cyano-azetidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-ethyl ester (7.75 g; 30.5 mmol) in methanol (1000 ml) is combined with wet RaNi (˜28 g) and hydrogenated at room temperature under 1 atm of hydrogen for 2 hours. The reaction mixture is filtered and evaporated to dryness to yield the title compound as light brown resin, which crystallizes slowly (6.8 g; 91%).

후처리

  1. filtrationThe reaction mixture is filtered
  2. customevaporated to dryness

출처 및 근거

ORD 기록
ord-378a6e0e38bf434db0c6f29381c8ff71
출처 데이터셋
uspto-grants-2010_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07838674B2

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