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Benzene → 4-Bromo-2-methyl-benzoic acid isopropyl ester

HRID 1869958
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HRID 1869958 반응식
[Br:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[C:4]([CH3:11])[CH:3]=1.S(=O)(=O)(O)O.O.[CH:18]1[CH:23]=CC=C[CH:19]=1>C(O)(C)C>[CH:18]([O:7][C:6](=[O:8])[C:5]1[CH:9]=[CH:10][C:2]([Br:1])=[CH:3][C:4]=1[CH3:11])([CH3:23])[CH3:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 241BenzeneHCID 962WaterHCID 1118Sulfuric AcidHCID 995704-Bromo-2-methylbenzoic acid

생성물 1

HCID 225688974-Bromo-2-methyl-benzoic acid isopropyl ester

시약·촉매·용매 1

HCID 3776Isopropanol용매

실험 절차

A solution of 4-bromo-2-methyl-benzoic acid (Aldrich, 5.4 g, 25 mmol) in benzene (75 mL) and isopropanol (75 mL) was treated with concentrated sulfuric acid (1.5 mL) and heated to reflux over 4 days using a Dean-Stark water trap. The volatiles were evaporated in vacuo, the residue was diluted with water and extracted with diethyl ether. The organic phase was washed with water and saturated, aqueous sodium bicarbonate solution, dried over anhydrous magnesium sulfate, filtered and evaporated in vacuo to afford the title product as a clear oil that was used as such for the next step (6.12 g, 95%).

후처리

  1. temperatureheated
  2. temperatureto reflux over 4 days
  3. customThe volatiles were evaporated in vacuo
  4. additionthe residue was diluted with water
  5. extractionextracted with diethyl ether
  6. washThe organic phase was washed with water
  7. dry with materialsaturated, aqueous sodium bicarbonate solution, dried over anhydrous magnesium sulfate
  8. filtrationfiltered
  9. customevaporated in vacuo

출처 및 근거

ORD 기록
ord-48430d04c4cb4a719a50a0bd2dae3779
출처 데이터셋
uspto-grants-2009_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07638648B2

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