3,5-Dimethoxybenzaldehyde → 3,5-Dimethoxy-1-(1-propenyl)benzene

HRID 24700

反応式

HRID 24700 の反応式
[Li][CH2:2][CH2:3]CC.[CH3:6][O:7][C:8]1[CH:9]=[C:10]([CH:13]=[C:14]([O:16][CH3:17])[CH:15]=1)[CH:11]=O>[Br-].C([P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)C.C1COCC1>[CH3:6][O:7][C:8]1[CH:9]=[C:10]([CH:11]=[CH:2][CH3:3])[CH:13]=[C:14]([O:16][CH3:17])[CH:15]=1

参加物

5

反応物 2

HCID 817473,5-DimethoxybenzaldehydeHCID 178418339Butyllithium

生成物 1

HCID 539005613,5-Dimethoxy-1-(1-propenyl)benzene

試薬・触媒・溶媒 2

HCID 73727Phosphonium, ethyltriphenyl-, bromide (1:1)触媒HCID 8028Tetrahydrofuran溶媒2 回

実験手順

Ethyltriphenylphosphonium bromide (4.69 g) was dissolved in anhydrous THF (70 mL) and the mixture cooled to 0-5° C. n-BuLi (5.05 mL of 2.5 M in hexane) was added dropwise and the resulting mixture was stirred at room temperature for 3 h. The mixture was cooled to −78° C. and a solution of 3,5-dimethoxybenzaldehyde (2 g) in anhydrous THF (14 mL) was added. The mixture was allowed to warm up to room temperature then stirred overnight. The mixture was concentrated, and the residue was taken up with AcOEt, washed with water and brine, dried (MgSO4), filtered and evaporated. The residue was purified by column chromatography (silica gel; eluent: hexane and AcOEt 10:1) to give 3,5-dimethoxy-1-(1-propenyl)benzene as a mixture of cis and trans isomers (2.15 g).

後処理

  1. additionwas added dropwise
  2. temperatureThe mixture was cooled to −78° C.
  3. temperatureto warm up to room temperature
  4. stirringthen stirred overnight
  5. concentrationThe mixture was concentrated
  6. washwashed with water and brine
  7. dry with materialdried (MgSO4)
  8. filtrationfiltered
  9. customevaporated
  10. customThe residue was purified by column chromatography (silica gel; eluent: hexane and AcOEt 10:1)

出典と根拠

ORDレコード
ord-e4d69c828dae4568959d5d61d5b064ec
出典データセット
uspto-grants-2005_02
特許番号
US06855843B2

関連ノート

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