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Tyramine hydrochloride → HCID 19363249, 화합물

HRID 850493
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HRID 850493 반응식
[CH2:1]([O:6][C:7]1[CH:8]=[C:9]([C:16]([OH:18])=O)[C:10](=[CH:14][CH:15]=1)[C:11]([OH:13])=O)[CH2:2][CH2:3][CH2:4][CH3:5].Cl.[NH2:20][CH2:21][CH2:22][C:23]1[CH:28]=[CH:27][C:26]([OH:29])=[CH:25][CH:24]=1>C(O)(=O)C>[OH:29][C:26]1[CH:27]=[CH:28][C:23]([CH2:22][CH2:21][N:20]2[C:16](=[O:18])[C:9]3=[CH:8][C:7]([O:6][CH2:1][CH2:2][CH2:3][CH2:4][CH3:5])=[CH:15][CH:14]=[C:10]3[C:11]2=[O:13])=[CH:24][CH:25]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 66449Tyramine hydrochlorideHCID 19363454HCID 19363454, 화합물

생성물 1

HCID 19363249HCID 19363249, 화합물수율 88%

시약·촉매·용매 1

HCID 176Acetic Acid용매

반응 조건

온도
96 °C

실험 절차

The crude product of 4-pentyloxyphthalic acid was dissolved in acetic acid (20 ml), and tyramine hydrochloride (2.74 g, 20 mmol) was added. The mixture was stirred at 96° C. for 4 hours, and concentrated under reduced pressure. The obtained residue was purified by column chromatography on silica gel (hexane/ethyl acetate=6/1) to give N-2-(4-hydroxyphenyl)ethyl-4-pentyloxyphthalimide (2.6 g, 9.4 mmol, 88%) as colorless crystals.

후처리

  1. concentrationconcentrated under reduced pressure
  2. customThe obtained residue was purified by column chromatography on silica gel (hexane/ethyl acetate=6/1)

출처 및 근거

ORD 기록
ord-3a17e233f62a4452b3a5d5a8a421f67c
출처 데이터셋
uspto-grants-2000_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06017919

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