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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrogen Bromide → Hydrogen Bromide

HRID 278164
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인쇄 미리보기

반응식

HRID 278164 반응식
C[O:2][C:3]1[CH:4]=[C:5]([CH2:9][CH2:10][CH:11]([NH2:18])[C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[CH:6]=[CH:7][CH:8]=1.[BrH:19]>CC(O)=O>[NH2:18][CH:11]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[CH2:10][CH2:9][C:5]1[CH:4]=[C:3]([OH:2])[CH:8]=[CH:7][CH:6]=1.[BrH:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 260Hydrogen BromideHCID 226271033-(3-Methoxyphenyl)-1-phenylpropylamine

생성물 2

HCID 260Hydrogen BromideHCID 226270983-(3-Amino-3-phenylpropyl)phenol

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

A mixture of the product from Step C (920 mg), HOAc (2 mL) and 48% HBr (3 mL) was stirred while heating at reflux. After 2-3 hours, the solution was concentrated in vacuo to provide a pale beige sticky solid which was triturated with Et2O. Removal of residual solvents in vacuo provided the titled product hydrobromide as a pale beige froth.

후처리

  1. temperaturewhile heating
  2. temperatureat reflux
  3. concentrationthe solution was concentrated in vacuo
  4. customto provide a pale beige sticky solid which
  5. customwas triturated with Et2O
  6. customRemoval of residual solvents in vacuo

출처 및 근거

ORD 기록
ord-0744501ef49e4ab5b29e01ccf689d3af
출처 데이터셋
uspto-grants-2002_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06358985B1

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