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

HRID 2412389
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반응식

HRID 2412389 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.[CH:18]1C=CC=C[CH:19]=1>C(O)C.S(=O)(=O)(O)O>[CH2:18]([O:10][C:9](=[O:11])[C:8]1[CH:12]=[CH:13][CH:14]=[CH:15][C:7]=1[O:6][C:5]1[CH:4]=[CH:3][C:2]([Br:1])=[CH:17][CH:16]=1)[CH3:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 241BenzeneHCID 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-bromophenoxy)benzoic acid in 1940 ml of absolute benzene, 218 ml of absolute ethanol and 32.6 ml of concentrated sulphuric acid is boiled under reflux for 32 hours, the water that forms being removed in a water separator. The reaction mixture is cooled to 10° and, with the addition of ice, is washed with 1000 ml of water, 500 ml of a 2N aqueous sodium carbonate solution and then once more with 1000 ml of water. The organic phase is separated off, dried over magnesium sulphate and concentrated by evaporation at 40° at a pressure of 11 mm Hg. The residue is distilled in a high vacuum and yields the 2-(4-bromophenoxy)benzoic acid ethyl ester. Boiling point 140°-150°/0.05 mm Hg.

후처리

  1. temperatureunder reflux for 32 hours
  2. customthe water that forms being removed in a water separator
  3. temperatureThe reaction mixture is cooled to 10° and, with the addition of ice
  4. washis washed with 1000 ml of water, 500 ml of a 2N aqueous sodium carbonate solution
  5. customThe organic phase is separated off
  6. dry with materialdried over magnesium sulphate
  7. concentrationconcentrated by evaporation at 40° at a pressure of 11 mm Hg
  8. distillationThe residue is distilled in a high vacuum

출처 및 근거

ORD 기록
ord-f38a308ee76d4700a228da6169edac94
출처 데이터셋
uspto-grants-1985_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04492691

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