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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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3-(Tetrahydro-furan-2-yl)-acrylonitrile → 3-(Tetrahydrofuran-2-yl)propan-1-amine

HRID 1822802
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HRID 1822802 반응식
[O:1]1[CH2:5][CH2:4][CH2:3][CH:2]1[CH:6]=[CH:7][C:8]#[N:9]>C1COCC1.[Ni]>[O:1]1[CH2:5][CH2:4][CH2:3][CH:2]1[CH2:6][CH2:7][CH2:8][NH2:9]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 695274123-(Tetrahydro-furan-2-yl)-acrylonitrile

생성물 1

HCID 221700413-(Tetrahydrofuran-2-yl)propan-1-amine수율 51%

시약·촉매·용매 2

HCID 935Nickel촉매HCID 8028Tetrahydrofuran용매

실험 절차

Raney Ni (approx 1 mL) was added to 3-(tetrahydro-furan-2-yl)-acrylonitrile (0.43 g, 3.5 mmol) in THF (6 mL), the mixture was evacuated then charged with 1 atm H2 (balloon) then stirred overnight. The mixture was recharged with Raney Ni (1 mL) and H2 and stirring was continued an additional 24 hour, until no starting material was evident via TLC. The reaction contents were filtered through a celite plug, that was thoroughly rinsed with MeOH, solvents removed to yield 3-(Tetrahydro-furan-2-yl)-propylamine (51% yield). ESI-MS (m/z) 130 [M+H]+.

후처리

  1. customthe mixture was evacuated
  2. additionthen charged with 1 atm H2 (balloon)
  3. stirringstirring
  4. waitwas continued an additional 24 hour, until no starting material
  5. customThe reaction contents
  6. filtrationwere filtered through a celite plug, that
  7. washwas thoroughly rinsed with MeOH, solvents
  8. customremoved

출처 및 근거

ORD 기록
ord-2ddd2bd9f72c448aa2b9c8b405b6cdd3
출처 데이터셋
uspto-grants-2006_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07037916B2

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