تفاعل #595298

ord-90b7e176bc064118b278806c0ba6dfbd

معادلة التفاعل

CC(=O)c1ccc(F)cc1F
2′,4′-difluoroacetophenone
CCOP(=O)(Cc1ccccc1Cl)OCC
diethyl 2-chlorobenzylphosphonate
[H-].[Na+]
sodium hydride
CC(=Cc1ccccc1Cl)c1ccc(F)cc1F
1-[1-(2-chlorophenyl)prop-1-en-2-yl]-2,4-difluorobenzene
المردود 26.0%

المذيبات

ظروف التفاعل

درجة الحرارة
3°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    غسيلfreshly washed with dry heptane) in dry DMF (20 ml)
  2. 2
    workup.STIRRINGThe resulting mixture was stirred at RT for 68 h
  3. 3
    استخلاصextracted with diethyl ether
  4. 4
    أخرىThe organic phase was dried
  5. 5
    تركيزconcentrated to dryness under reduced pressure
  6. 6
    أخرىthe residue was purified by chromatography on silica gel, which

الإجراء التجريبي

At 3° C., a solution of diethyl 2-chlorobenzylphosphonate (2.00 g, 7.61 mmol) in dry DMF (30 ml) was added to a stirred suspension of sodium hydride (60% by weight suspension in mineral oil, 365 mg, 9.13 mmol; freshly washed with dry heptane) in dry DMF (20 ml). After 1 h of stirring at 3° C., a solution of 2′,4′-difluoroacetophenone (1.31 g, 8.37 mmol) in dry DMF (20 ml) was added dropwise. The resulting mixture was stirred at RT for 68 h and then diluted with water and extracted with diethyl ether. The organic phase was dried and concentrated to dryness under reduced pressure, and the residue was purified by chromatography on silica gel, which gave 1-[1-(2-chlorophenyl)prop-1-en-2-yl]-2,4-difluorobenzene as a 93/7 mixture of diastereoisomers [colourless solid, 560 mg, yield 26%; GC/MS: m/z=264 (M+); HPLC/MS: log P(HCOOH)=5.05 (major diastereoisomer), 5.34 (minor diastereoisomer)].

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09095136B2uspto-grants-2015_08