Bromoacetic Acid → ((4-Phenylbutyl)hydroxyphosphoryl)acetic acid

Temperatur

0 °C

To a solution of 4-phenylbutyl phosphonous acid (0.5 g, 0.002525 mole) in chloroform (10 ml) was added triethylamine (1.16 ml, 0.00833 mole) and the solution was cooled in an ice bath to 0° C. Trimethyl silyl chloride (1.06 ml, 0.00833 mole) was added to the above solution dropwise, followed by bromoacetic acid (0.36 g, 0.00277 mole). The ice bath was removed and the mixture stirred at room temperature for 3 hours and poured into 10% aqueous HCl (30 ml) and crushed ice (20 g). After shaking the mixture in a separatory funnel, the chloroform layer was separated and the aqueous layer extracted with dichloromethane (2×50 ml). The combined organic phase was washed with brine, dried over anhydrous sodium sulfate and the solvents removed on a rotavap. The resulting crude thick oil (0.6 g) was dissolved in 30 ml ether; hexane was added dropwise to get a turbid solution and left at room temperature overnight to complete the crystallization. The resulting product was cooled in the freezer for 12 hours, filtered and the solid was washed very thoroughly with hexane (50 ml), ether (50 ml) and again very thoroughly with hexane (50 ml), ether (50 ml) in that order. The solid was vacuum dried to get 0.5 g (83%) of title compound.

1. customThe ice bath was removed
2. additionpoured into 10% aqueous HCl (30 ml)
3. customcrushed ice (20 g)
4. stirringAfter shaking the mixture in a separatory funnel
5. customthe chloroform layer was separated
6. extractionthe aqueous layer extracted with dichloromethane (2×50 ml)
7. washThe combined organic phase was washed with brine
8. dry with materialdried over anhydrous sodium sulfate
9. customthe solvents removed on a rotavap
10. dissolutionThe resulting crude thick oil (0.6 g) was dissolved in 30 ml ether
11. additionhexane was added dropwise
12. customto get a turbid solution
13. waitleft at room temperature overnight
14. customthe crystallization
15. temperatureThe resulting product was cooled in the freezer for 12 hours
16. filtrationfiltered
17. washthe solid was washed very thoroughly with hexane (50 ml), ether (50 ml) and again very thoroughly with hexane (50 ml), ether (50 ml) in that order
18. customdried

ORD-Eintrag

ord-0f6464d4befc42a1ab373b3b00e3e783

Quelldatensatz

uspto-grants-1986_07

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US04602092