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Hydrogen Bromide → 113884-76-7

HRID 2231507
ノート
印刷プレビュー

反応式

HRID 2231507 の反応式
Cl.C[O:3][C:4]1[CH:5]=[C:6]2[C:11](=[CH:12][C:13]=1[O:14]C)[CH:10]=[N:9][CH:8]=[CH:7]2.[BrH:16]>>[BrH:16].[OH:3][C:4]1[CH:5]=[C:6]2[C:11](=[CH:12][C:13]=1[OH:14])[CH:10]=[N:9][CH:8]=[CH:7]2
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 260Hydrogen BromideHCID 212868646,7-Dimethoxyisoquinoline hydrochloride

生成物 1

HCID 135736659113884-76-7収率 97.6%

実験手順

63.4 g (0.28 mol) of 6,7-dimethoxyisoquinoline hydrochloride was dissolved in 630 ml of 47% hydrobromic acid, and the mixture was refluxed for 24 hours under stirring in nitrogen atmosphere. The reaction mixture was allowed to stand still under cooling with ice. The crystals formed were collected by filtration and washed with cold water and acetone. They were dried in air overnight and then dried at a temperature of from 90° to 95° C. for 6 hours to obtain 66.4 g (yield: 97.6%) of the above identified compound.

後処理

  1. temperaturethe mixture was refluxed for 24 hours
  2. temperatureunder cooling with ice
  3. customThe crystals formed
  4. filtrationwere collected by filtration
  5. washwashed with cold water and acetone
  6. customThey were dried in air overnight
  7. customdried at a temperature of from 90° to 95° C. for 6 hours
  8. customto obtain 66.4 g (yield: 97.6%) of the

出典と根拠

ORDレコード
ord-b1790ec008744d5cac8ad4aa2ffd039b
出典データセット
uspto-grants-1988_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04782155

反応ノート

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