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p-Toluenesulfonic acid → 1-Bromo-2-(1E)-1-propen-1-ylbenzene

HRID 2297734
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HRID 2297734 반응식
C1(C)C=CC(S(O)(=O)=O)=CC=1.[Br:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=1[CH:19](O)[CH2:20][CH3:21].C(=O)(O)[O-].[Na+]>C1(C)C=CC=CC=1>[CH:19](/[C:14]1[CH:15]=[CH:16][CH:17]=[CH:18][C:13]=1[Br:12])=[CH:20]\[CH3:21]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6101p-Toluenesulfonic acidHCID 516892Sodium BicarbonateHCID 134442791-(2-Bromophenyl)-1-propanol

생성물 1

HCID 127154371-Bromo-2-(1E)-1-propen-1-ylbenzene수율 803.4%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

p-Toluenesulfonic acid (30 mg) was added to a solution (50 mL) of 1-(2-bromophenyl)-1-propanol (5.55 g, 3.0 mmol) in toluene, followed by reflux for 5 hours. Next, the reaction solution was added to a saturated aqueous solution of sodium bicarbonate under ice-cooling to neutralize the reaction solution, and the mixture was then extracted with diethyl ether. After the extract was washed with a saturated brine and then dried over sodium sulfate, the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (developed with diethyl ether/hexane=1/10) to give 2-((E)-1-propenyl)bromobenzene (4.75 g, yield 100%).

후처리

  1. temperatureby reflux for 5 hours
  2. temperaturecooling
  3. extractionthe mixture was then extracted with diethyl ether
  4. washAfter the extract was washed with a saturated brine
  5. dry with materialdried over sodium sulfate
  6. customthe solvent was evaporated under reduced pressure
  7. customThe obtained residue was purified by silica gel column chromatography (developed with diethyl ether/hexane=1/10)

출처 및 근거

ORD 기록
ord-7c180e5da27e43988a7462a41badf644
출처 데이터셋
uspto-grants-2002_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06492392B1

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