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Ethanol → 4-(2-Aminoethyl)-3-methoxymethoxyphenol

HRID 1351767
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HRID 1351767 반응식
C([O:8][C:9]1[CH:14]=[CH:13][C:12]([CH2:15][CH2:16][NH2:17])=[C:11]([O:18][CH3:19])[C:10]=1OC)C1C=CC=CC=1.[CH2:22]([OH:24])C>[Pd]>[NH2:17][CH2:16][CH2:15][C:12]1[CH:13]=[CH:14][C:9]([OH:8])=[CH:10][C:11]=1[O:18][CH2:19][O:24][CH3:22]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 702EthanolHCID 109681642-(4-Benzyloxy-2-methoxy-methoxyphenyl)ethylamine

생성물 1

HCID 178562194-(2-Aminoethyl)-3-methoxymethoxyphenol

시약·촉매·용매 1

HCID 23938Palladium촉매

실험 절차

A mixture of 18.00 g of 2-(4-benzyloxy-2-methoxy-methoxyphenyl)ethylamine, 3.6 g of 10% palladium on carbon (Degussa Inc.: E101 NE/W) and 230 mL of ethanol was stirred under a hydrogen atmosphere at room temperature for 1 hour. After the catalyst was filtered off through a diatomaceous earth, the filtrate was concentrated under reduced pressure to give 12.65 g of 4-(2-aminoethyl)-3-methoxymethoxyphenol as a colorless solid.

후처리

  1. filtrationAfter the catalyst was filtered off through a diatomaceous earth
  2. concentrationthe filtrate was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-709c9e234cbd4f06a5e75952f381ed99
출처 데이터셋
uspto-grants-2007_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07217832B2

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