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Triphenylphosphine → 1-(3-Methylpyridin-2-yl)ethan-1-amine

HRID 251204
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HRID 251204 반응식
[N:1]([CH:4]([C:6]1[C:11]([CH3:12])=[CH:10][CH:9]=[CH:8][N:7]=1)[CH3:5])=[N+]=[N-].C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>C1COCC1>[CH3:12][C:11]1[C:6]([CH:4]([NH2:1])[CH3:5])=[N:7][CH:8]=[CH:9][CH:10]=1
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참가 물질

4

반응물 2

HCID 11776TriphenylphosphineHCID 914713542-(1-Azido-ethyl)-3-methyl-pyridine

생성물 1

HCID 457911661-(3-Methylpyridin-2-yl)ethan-1-amine수율 76.4%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

A solution of the above azide (254 mg, 1.57 mmol) and PPh3 (828 mg, 3.16 mmol) in 10% aqueous THF (10 mL) was stirred at room temperature for 15 hours. The solvent was removed under reduced pressure and the residue was purified by flash column chromatography on silica (CH2Cl2/MeOH, 9:1), giving 1-(3-methyl-pyridin-2-yl)-ethylamine as a yellow liquid (163 mg, 1.20 mmol, 76%). 1H NMR (CDCl3) δ 1.35 (d, 3H, J=6.6 Hz), 2.00 (s, 2H), 2.33 (s, 3H), 4.30 (q, 1H, J=6.6 Hz), 7.05 (dd, 1H, J=7.5, 4.8 Hz), 7.40 (d, 1H, J=7.5 Hz), 8.41 (d, 1H, J=4.2 Hz).

후처리

  1. customThe solvent was removed under reduced pressure
  2. customthe residue was purified by flash column chromatography on silica (CH2Cl2/MeOH, 9:1)

출처 및 근거

ORD 기록
ord-a3eaf16692a04a948bffd7058437286f
출처 데이터셋
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07863293B2

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