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3-(N-Methyl-N-phenylamino)-2-hydroxypropylazide → 1-Amino-3-[methyl(phenyl)amino]propan-2-ol

HRID 1901738
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인쇄 미리보기

반응식

HRID 1901738 반응식
[H][H].[CH3:3][N:4]([CH2:11][CH:12]([OH:17])[CH2:13][N:14]=[N+]=[N-])[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1>[Pd].C(O)C>[CH3:3][N:4]([CH2:11][CH:12]([OH:17])[CH2:13][NH2:14])[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 214747453-(N-Methyl-N-phenylamino)-2-hydroxypropylazideHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 2725791-Amino-3-[methyl(phenyl)amino]propan-2-ol수율 99%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

Hydrogen was introduced into a mixture of 1.85 g of 3-(N-methyl-N-phenylamino)-2-hydroxypropylazide (prepared as described in Preparation 89), 0.9 g of 10% w/w palladium-on-carbon and 30 ml of ethanol for 1.5 hours. At the end of this time, the atmosphere was replaced with nitrogen, the palladium-on-carbon catalyst was removed from the reaction mixture by filtration, and the filtrate was concentrated by evaporation under reduced pressure, to give 1.6 g of the title compound which decomposed at 136° C.

후처리

  1. customthe palladium-on-carbon catalyst was removed from the reaction mixture by filtration
  2. concentrationthe filtrate was concentrated by evaporation under reduced pressure

출처 및 근거

ORD 기록
ord-0fad934a0c6d4bb6868b47aec2ad675e
출처 데이터셋
uspto-grants-1996_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05578620

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