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

HRID 2297734
ノート
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反応式

HRID 2297734 の反応式
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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

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%).

後処理

  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)

出典と根拠

ORDレコード
ord-7c180e5da27e43988a7462a41badf644
出典データセット
uspto-grants-2002_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06492392B1

反応ノート

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