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Triphenylphosphine → 1-[(E)-3-bromo-1-methyl-1-propenyl]-3-nitrobenzene

HRID 1826402
ノート
印刷プレビュー

反応式

HRID 1826402 の反応式
C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[Br:20]Br.[N+:22]([C:25]1[CH:26]=[C:27](/[C:31](/[CH3:35])=[CH:32]/[CH2:33]O)[CH:28]=[CH:29][CH:30]=1)([O-:24])=[O:23]>C(#N)C>[Br:20][CH2:33]/[CH:32]=[C:31](/[C:27]1[CH:28]=[CH:29][CH:30]=[C:25]([N+:22]([O-:24])=[O:23])[CH:26]=1)\[CH3:35]
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 11776TriphenylphosphineHCID 24408BromineHCID 69554909(E)-3-(3-nitrophenyl)-2-buten-1-ol

生成物 1

HCID 695548111-[(E)-3-bromo-1-methyl-1-propenyl]-3-nitrobenzene

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒3 回

実験手順

To a solution of triphenylphosphine (5.15 g, 19.7 mmol) in acetonitrile (140 ml) was added dropwise over 5 minutes a solution of bromine (3.15 g, 19.7 mmol) in acetonitrile (5 ml) at a rate such that the temperature did not exceed −10° C. The mixture was allowed to warm to room temperature, then to this was added a solution of (E)-3-(3-nitrophenyl)-2-buten-1-ol (Preparation 2, 4 g, 20.7 mmol) in acetonitrile (5 ml). The mixture was warmed gently to 65° C. for 1 h, cooled to room temperature and then poured onto diethyl ether (50 ml). The mixture was concentrated in vacuo, then diethyl ether (200 ml) was added. The mixture was filtered, concentrated again in vacuo and the residue purified by silica column (300 g) chromatography, eluting with 3:1 hexane/dichloromethane then 1:1 hexane/dichloromethane. Appropriate fractions were combined and concentrated in vacuo to give the title compound as a very pale yellow oil (4 g, 75%).

後処理

  1. customdid not exceed −10° C
  2. temperatureThe mixture was warmed gently to 65° C. for 1 h
  3. temperaturecooled to room temperature
  4. additionpoured onto diethyl ether (50 ml)
  5. concentrationThe mixture was concentrated in vacuo
  6. additiondiethyl ether (200 ml) was added
  7. filtrationThe mixture was filtered
  8. concentrationconcentrated again in vacuo
  9. customthe residue purified by silica column (300 g) chromatography
  10. washeluting with 3:1 hexane/dichloromethane
  11. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-09856ba663cd48cc9d2fd6f51612900e
出典データセット
uspto-grants-2006_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07049444B2

反応ノート

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