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Bromine → Ethyl 2-bromo-5-ethoxy-4-methylbenzoate

HRID 402764
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HRID 402764 반응식
[CH2:1]([O:3][C:4]1[C:5]([CH3:15])=[CH:6][CH:7]=[C:8]([CH:14]=1)[C:9]([O:11][CH2:12][CH3:13])=[O:10])[CH3:2].[Br:16]Br>C(O)(=O)C.O>[Br:16][C:7]1[CH:6]=[C:5]([CH3:15])[C:4]([O:3][CH2:1][CH3:2])=[CH:14][C:8]=1[C:9]([O:11][CH2:12][CH3:13])=[O:10]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 24408BromineHCID 23136282Ethyl 3-ethoxy-4-methylbenzoate

생성물 1

HCID 66764786Ethyl 2-bromo-5-ethoxy-4-methylbenzoate수율 92.9%

시약·촉매·용매 2

HCID 176Acetic Acid용매HCID 962Water용매

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온도
60 °C

실험 절차

To a solution of ethyl 5-ethoxy-4-methylbenzoate (500 mg, 2.40 mmol) in acetic acid (10 mL) and water (10 mL) at room temperature was added bromine (385 mg, 2.40 mmol). The resulting reaction mixture was stirred at 60° C. for 1 hour. After cooling to room temperature, the reaction mixture was diluted with hexanes/ether (80/20). Layers were separated and the organic layer was washed with saturated Na2CO3, brine, dried over Na2SO4, filtered and concentrated. The residue was purified on a silica gel column eluting with 5 to 10% EtOAc in hexanes to yield the title intermediate (660 mg, 2.23 mmol) as light yellow solid.

후처리

  1. customThe resulting reaction mixture
  2. temperatureAfter cooling to room temperature
  3. customLayers were separated
  4. washthe organic layer was washed with saturated Na2CO3, brine
  5. dry with materialdried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customThe residue was purified on a silica gel column
  9. washeluting with 5 to 10% EtOAc in hexanes

출처 및 근거

ORD 기록
ord-a48448456db547b6b2aaeb906af84537
출처 데이터셋
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08742110B2

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