Benzoyl Peroxide → Methyl 4-(diethoxyphosphorylmethyl)benzoate

To a solution of methyl 4-methylbenzoate (2.01 g, 13.3 mmol) and 1,2-dichloroethane (100 mL) was added benzoyl peroxide (catalytic amount) and NBS (2.84 g, 16.0 mmol). The resulting mixture was heated to reflux while being stirred under nitrogen. After three hours, another catalytic amount of benzoyl peroxide was added and the mixture was refluxed for an additional three hours. The reaction mixture was allowed to cool to RT, followed by the addition of Et2O (20 mL) and filtration of a solid which precipitated out of solution. The filtrate was washed with water (2×) and brine (2×), dried over MgSO4, filtered and the solvent was removed under reduced pressure to give a light yellow clear oil. Triethyl phosphite (2.28 mL, 13.3 mmol) was added to the oil and the reaction was stirred under nitrogen at 160° C. for three hours. Excess triethyl phosphite was distilled off and the product was purified by column chromatography (EtOAc) to give a transparent light yellow oil (2.28 g, 7.97 mmol, 60%). Characterization data matches literature. E. N. Durantini, Synthetic Communications, 29:4201-4222 (1999).

1. temperatureThe resulting mixture was heated
2. temperatureto reflux
3. temperaturethe mixture was refluxed for an additional three hours
4. customprecipitated out of solution
5. washThe filtrate was washed with water (2×) and brine (2×)
6. dry with materialdried over MgSO4
7. filtrationfiltered
8. customthe solvent was removed under reduced pressure
9. customto give a light yellow clear oil
10. stirringthe reaction was stirred under nitrogen at 160° C. for three hours
11. distillationExcess triethyl phosphite was distilled off
12. customthe product was purified by column chromatography (EtOAc)

ORD record

ord-64ed2f31f84c4378a90d2c7ac36ab705

Source dataset

uspto-grants-2016_05

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US09334304B2