تفاعل #347275

ord-3d72fe12dff1440c9af3da10a0d89a39

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONdispersed
  2. 2
    workup.ADDITIONtherein was added
  3. 3
    أخرىreacted for 15 hours at room temperature
  4. 4
    أخرىThe reaction liquid
  5. 5
    workup.ADDITIONwas added
  6. 6
    استخلاصthe resulting liquid was extracted with dichloromethane
  7. 7
    تجفيفThe extract was dried with anhydrous sodium sulfate
  8. 8
    تركيزconcentrated
  9. 9
    أخرىpurified by silica gel column chromatography diethyl (ether:hexane--1:2 by volume)

الإجراء التجريبي

1.0 g of 3-nitro-4-chlorobenzaldehyde and 2.8 g of 3,4,5-trimethoxybenzyltriphenylphosphine bromide were dissolved in 50 ml of benzene, and a benzene solution containing 260 mg of sodium hydride dispersed therein was added thereto and reacted for 15 hours at room temperature. The reaction liquid 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 diethyl (ether:hexane--1:2 by volume) to obtain 0.95 g of the intended compound. The yield of the product was 50.4%.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05525632uspto-grants-1996_06