تفاعل #319066
ord-a2ebce2b9ce046349ce522148bdf6ab2
معادلة التفاعل
المتفاعلات
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1تركيزafter which it was concentrated in vacuo
- 2workup.STIRRINGThe resulting yellow mixture was stirred overnight at 65° C.
- 3أخرىresulting in an orange semisolid
- 4غسيلwashed sequentially with 1N hydrochloric acid and saturated sodium bicarbonate solution
- 5تجفيفdried (MgSO4)
- 6تركيزconcentrated to an orange oil
- 7غسيلeluting with a gradient from 1:1 hexane
الإجراء التجريبي
A solution of (4-phenylbutyl)-phosphinic acid, ethyl ester (8.0 g, 35.4 mmols) in chloroform (40 ml) were added trimethylsilyl chloride (13.5 ml, 106 mmols) and triethylamine (19.7 ml, 142 mmols). The resulting mixture was stirred at 25° C. for 2.5 hours, after which it was concentrated in vacuo. To the residue were added methyl α-chloro=acrylate (20 g, 0.16 mole, prepared as described by C. S. Marvel and J. C. Cowan, J. Amer. Chem. Soc. 61, 3156 (1939)) and triethylamine (9.0 ml, 64 mmol). The resulting yellow mixture was stirred overnight at 65° C., resulting in an orange semisolid. The mixture was diluted with ethyl acetate and washed sequentially with 1N hydrochloric acid and saturated sodium bicarbonate solution, dried (MgSO4), and concentrated to an orange oil. The oil was chromotographed on LPS-1 silica gel, eluting with a gradient from 1:1 hexane:ethyl acetate to ethyl acetate, to give the title compound.