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Ethanol → Ethyl 7-bromo-3-hydroxy-2-naphthoate

HRID 2187646
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HRID 2187646 반응식
[Br:1][C:2]1[CH:11]=[C:10]2[C:5]([CH:6]=[C:7]([OH:15])[C:8]([C:12]([OH:14])=[O:13])=[CH:9]2)=[CH:4][CH:3]=1.O.C([O-])(O)=O.[Na+].[CH3:22][CH2:23]O>S(=O)(=O)(O)O>[CH2:22]([O:13][C:12]([C:8]1[C:7]([OH:15])=[CH:6][C:5]2[C:10](=[CH:11][C:2]([Br:1])=[CH:3][CH:4]=2)[CH:9]=1)=[O:14])[CH3:23]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 702EthanolHCID 962WaterHCID 745032-Naphthalenecarboxylic acid, 7-bromo-3-hydroxy-HCID 516892Sodium Bicarbonate

생성물 1

HCID 18476207Ethyl 7-bromo-3-hydroxy-2-naphthoate수율 85%

시약·촉매·용매 1

HCID 1118Sulfuric Acid용매

실험 절차

A solution of 81 g (0.3 mol) of 7-bromo-3-hydroxy-2-naphthoic acid in 600 ml dried EtOH and 60 ml conc. sulfuric acid was heated at reflux for 16 hours. The mixture was cooled to room temperature and treated with water (4000 ml) and neutralised with NaHCO3. The solid was separated by filtration and dried in a drying chamber afforded 75.3 g (85%) of the titled compound.

후처리

  1. temperatureat reflux for 16 hours
  2. customThe solid was separated by filtration
  3. customdried in a drying chamber

출처 및 근거

ORD 기록
ord-f978a3687f9544378fc42058e1d9924b
출처 데이터셋
uspto-grants-2002_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06410562B1

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