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Ethanol → Ethyl 4-bromo-3-methylbenzoate

HRID 340285
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HRID 340285 반응식
[Br:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][C:3]=1[CH3:11].S(Cl)(Cl)=O.[CH3:16][CH2:17]O>>[Br:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([O:8][CH2:16][CH3:17])=[O:7])=[CH:4][C:3]=1[CH3:11]
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참가 물질

4

반응물 3

HCID 702EthanolHCID 24386Thionyl ChlorideHCID 821314-Bromo-3-methylbenzoic acid

생성물 1

HCID 21729626Ethyl 4-bromo-3-methylbenzoate

실험 절차

To a solution of 4-bromo-3-methylbenzoic acid (commercially available) (1.0 eq.) in EtOH (0.3 M) was added thionyl chloride (1.5 eq.) and heated to reflux for 2 hours. The solvent was concentrated en vacuo, and the residue was diluted in ether and neutralized with saturated aqueous sodium bicarbonate solution. The two phases were separated, and the aqueous layer was extracted with ether. The combined organic layers were washed with brine, dried over anhydrous MgSO4, and concentrated en vacuo to give ethyl 4-bromo-3-methylbenzoate.

후처리

  1. temperatureheated
  2. temperatureto reflux for 2 hours
  3. concentrationThe solvent was concentrated en vacuo
  4. additionthe residue was diluted in ether and neutralized with saturated aqueous sodium bicarbonate solution
  5. customThe two phases were separated
  6. extractionthe aqueous layer was extracted with ether
  7. washThe combined organic layers were washed with brine
  8. dry with materialdried over anhydrous MgSO4
  9. concentrationconcentrated en vacuo

출처 및 근거

ORD 기록
ord-6ff0f0b8a91e4a0ba917b901c448c6e7
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08895577B2

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