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Benzene → Ethyl 2-(4-bromo-phenoxy)-benzoate

HRID 444235
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HRID 444235 반응식
[Br:1][C:2]1[CH:17]=[CH:16][C:5]([O:6][C:7]2[CH:15]=[CH:14][CH:13]=[CH:12][C:8]=2[C:9]([OH:11])=[O:10])=[CH:4][CH:3]=1.O.[CH:19]1C=CC=C[CH:20]=1>C(O)C.S(=O)(=O)(O)O>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([O:6][C:7]2[CH:15]=[CH:14][CH:13]=[CH:12][C:8]=2[C:9]([O:11][CH2:19][CH3:20])=[O:10])=[CH:16][CH:17]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 241BenzeneHCID 962WaterHCID 19803169HCID 19803169, 화합물

생성물 1

HCID 23464800Ethyl 2-(4-bromo-phenoxy)-benzoate

시약·촉매·용매 2

HCID 702Ethanol용매HCID 1118Sulfuric Acid용매

실험 절차

A mixture of 560.0 g of 2-(4-bromo-phenoxy)benzoic acid in 1,940 ml of absolute benzene, 218 ml of absolute ethanol and 32.6 ml of concentrated sulfuric acid is refluxed for 32 hours, the water formed being removed in a water separator. The reaction mixture is cooled to 10° and washed, with the addition of ice, with 1,000 ml of water, 500 ml of a 2 N aqueous sodium carbonate solution and then again with 1,000 ml of water. The organic phase is separated off, dried over magnesium sulfate and evaporated at 40° under a pressure of 11 mm Hg. The residue is distilled under a high vacuum and yields ethyl 2-(4-bromo-phenoxy)-benzoate, boiling point 140°-150°/0.05 mm Hg.

후처리

  1. temperatureis refluxed for 32 hours
  2. custombeing removed in a water separator
  3. temperatureThe reaction mixture is cooled to 10°
  4. washwashed, with the addition of ice, with 1,000 ml of water, 500 ml of a 2 N aqueous sodium carbonate solution
  5. customThe organic phase is separated off
  6. dry with materialdried over magnesium sulfate
  7. customevaporated at 40° under a pressure of 11 mm Hg
  8. distillationThe residue is distilled under a high vacuum

출처 및 근거

ORD 기록
ord-9b8ac4588c854dcaa958b810860e9912
출처 데이터셋
uspto-grants-1981_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04263315

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