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Water → 5-Bromo-2-methoxyphenol

HRID 1736497
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Reaction equation

HRID 1736497 reaction equation
[C:1]([O:9][C:10]1[CH:15]=[CH:14][C:13]([Br:16])=[CH:12][C:11]=1[O:17]C)(=O)C1C=CC=CC=1.[OH-].[Na+].O>C(O)C>[Br:16][C:13]1[CH:14]=[CH:15][C:10]([O:9][CH3:1])=[C:11]([OH:17])[CH:12]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 962WaterHCID 14798Sodium HydroxideHCID 53657601HCID 53657601, compound

Product 1

HCID 1422285-Bromo-2-methoxyphenolYield 98.3%

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

A mixture of 4-bromo-2-methoxyphenyl benzoate (5 g), sodium hydroxide (3 g), water (5 mL) and ethanol (50 mL) is heated at reflux for 1.5 hours. It is then evaporated to low bulk and the resulting residue is treated with water (20 mL) and concentrated hydrochloric acid (10 mL), and extracted with dichloromethane (150 mL). The organic solution is extracted with saturated aqueous sodium bicarbonate solution (3×25 mL), dried over magnesium sulphate and evaporated, to give 5-bromo-2-methoxyphenol (3.25 g), in the form a colorless solid, m.p. 67°-68° C. [Elemental analysis: C,41.5; H,3.5; Br, 37.8%; calculated: C,41.6; H,3.5; Br, 39.5%].

Workup

  1. temperatureis heated
  2. temperatureat reflux for 1.5 hours
  3. customIt is then evaporated to low bulk
  4. additionthe resulting residue is treated with water (20 mL) and concentrated hydrochloric acid (10 mL)
  5. extractionextracted with dichloromethane (150 mL)
  6. extractionThe organic solution is extracted with saturated aqueous sodium bicarbonate solution (3×25 mL)
  7. dry with materialdried over magnesium sulphate
  8. customevaporated

Sources & evidence

ORD record
ord-e0f44e73107247df9ef78aa1f2629230
Source dataset
uspto-grants-1996_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05541219

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes