Isopropanol → 1,3-Dichloro-1,1,2,2,3-pentafluoropropane

1,1,3-trichloro-1,2,2,3,3-pentafluoropropane(produced in Part C above) (106.6 g, 0.45 mol) and 300 g(5 mol) isopropanol were stirred under an inert atmosphere and irradiated 4.5 hours with a 450 W Hanovia Hg lamp at a distance of 2-3 inches(5-7.6 cm). The acidic reaction mixture was then poured into 1.5 liters ice water. The organic layer was separated, washed twice with 50 ml water, dried with calcium sulfate, and distilled to give 50.5 g ClCF2CF2CHClF, bp 54.5°-56° C. (55%). 1H NMR (CDCl3): ddd centered at 6.43 ppm. J H--C--F=47 Hz, J H--C--C--Fa=12 Hz, J H--C--C--Fb=2 Hz.

1. customirradiated 4.5 hours with a 450 W Hanovia Hg lamp at a distance of 2-3 inches(5-7.6 cm)
2. customThe organic layer was separated
3. washwashed twice with 50 ml water
4. dry with materialdried with calcium sulfate
5. distillationdistilled

ORD-Eintrag

ord-56e2ac0045884bf3a2623a6c8c2be509

Quelldatensatz

uspto-grants-1994_02

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US05288819