Water → HCID 19009247, compound

5.8 g of 2,5-dimethoxy-3,4,6-trimethylphenol [prepared as described in step (a) above] in 10 ml of dimethylformamide were added to a suspension of 1.4 g of sodium hydride (as a 55% w/w dispersion in mineral oil) in 50 ml of dimethylformamide, whilst ice-cooling, and the mixture was stirred at room temperature for 2 hours. At the end of this time, a solution of 4.6 g of p-fluoronitrobenzene in 10 ml of dimethylformamide was added to the mixture, whilst ice-cooling. The mixture was then stirred at room temperature for 1 hour, and then at 80° C. for 7 hours. At the end of this time, the mixture was poured into water, and the resulting crude oil was extracted with benzene. The benzene extract was washed with water and dried over anhydrous sodium sulfate. The solvent was then removed by distillation under reduced pressure, and the resulting oil was purified by column chromatography through silica gel, using a 4:1 by volume mixture of benzene and hexane, followed by benzene alone, as the eluent, to give 3.9 g of the title compound.

1. temperaturewhilst ice-cooling
2. temperaturecooling
3. stirringThe mixture was then stirred at room temperature for 1 hour
4. waitat 80° C. for 7 hours
5. extractionthe resulting crude oil was extracted with benzene
6. extractionThe benzene extract
7. washwas washed with water
8. dry with materialdried over anhydrous sodium sulfate
9. customThe solvent was then removed by distillation under reduced pressure
10. customthe resulting oil was purified by column chromatography through silica gel
11. additionby volume mixture of benzene and hexane

ORD record

ord-bda9f57ac84c46869eaa4f10e64b6162

Source dataset

uspto-grants-1994_08

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US05338855