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1-(2-Nitrobenzyl)pyrrolidine → HCID 89314201, 화합물

HRID 239200
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반응식

HRID 239200 반응식
[N+:1]([C:4]1[CH:15]=[CH:14][CH:13]=[CH:12][C:5]=1[CH2:6][N:7]1[CH2:11][CH2:10][CH2:9][CH2:8]1)([O-])=[O:2]>CN1CCOCC1.[Pt]>[CH2:9]1[CH2:8][N:7]([CH2:6][C:5]2[C:4]([NH:1][OH:2])=[CH:15][CH:14]=[CH:13][CH:12]=2)[CH2:11][CH2:10]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 2643101-(2-Nitrobenzyl)pyrrolidine

생성물 1

HCID 89314201HCID 89314201, 화합물

시약·촉매·용매 2

HCID 23939Platinum촉매HCID 79724-Methylmorpholine용매

실험 절차

The N-(2-nitrobenzyl)-pyrrolidine (20 mmol) was dissolved in N-methyl-morpholine (20 ml). Platinum on carbon (5 mol-%, 0.17 mmol, 350 mg, Degussa Type F105 RS/W) was added. The reaction vessel was evacuated and flushed with nitrogen three times, before a hydrogen atmosphere was applied. Thin layer chromatography control showed complete consumption of the starting material after 4 hours. The platinum catalyst was removed by filtration over celite. The crude product was obtained after evaporation of all volatiles under reduced pressure in a purity of >90%, as measured by 1H NMR.

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  1. customThe reaction vessel was evacuated
  2. customflushed with nitrogen three times, before a hydrogen atmosphere
  3. customconsumption of the starting material after 4 hours
  4. customThe platinum catalyst was removed by filtration over celite

출처 및 근거

ORD 기록
ord-cc5da4cdbb4c45e2b4367a256315a325
출처 데이터셋
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08642780B2

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