반응 #347273

ord-e7bc58f006fb4be784d38370b9d81678

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONdispersed
  2. 2
    workup.ADDITIONtherein was added
  3. 3
    기타reacted for 15 hours at room temperature (about 20°-30° C.)
  4. 4
    workup.ADDITIONwas added
  5. 5
    추출the resulting liquid was extracted with dichloromethane
  6. 6
    건조The extract was dried with anhydrous sodium sulfate
  7. 7
    농축concentrated
  8. 8
    기타purified by silica gel column chromatography (ethyl acetate:hexane=1:2 by volume)

실험 절차

1.54 g of 3-nitro-4-methoxybenzaldehyde and 4.45 g of 3,4,5-trimethoxybenzyltriphenylphosphine bromide were dissolved in 40 ml of benzene, and a benzene solution containing 408 mg of sodium hydride dispersed therein was added thereto and reacted for 15 hours at room temperature (about 20°-30° C.). The reaction mixture was neutralized with acetic acid, saturated sodium chloride solution was added thereto, and the resulting liquid was extracted with dichloromethane. The extract was dried with anhydrous sodium sulfate, concentrated and then purified by silica gel column chromatography (ethyl acetate:hexane=1:2 by volume) to obtain 1.27 g of the intended compound. The yield of the product was 43%.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05525632uspto-grants-1996_06