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Water → 5-Bromo-2-methoxyphenol

HRID 1736497
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HRID 1736497 반응식
[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
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참가 물질

5

반응물 3

HCID 962WaterHCID 14798Sodium HydroxideHCID 53657601HCID 53657601, 화합물

생성물 1

HCID 1422285-Bromo-2-methoxyphenol수율 98.3%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

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%].

후처리

  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

출처 및 근거

ORD 기록
ord-e0f44e73107247df9ef78aa1f2629230
출처 데이터셋
uspto-grants-1996_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05541219

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