Welcome to chemicalbook!
Chinese English Japanese Germany Korea
010-86108875
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

1415108-26-7

7-BROMO-4,4-DIFLUORO-3,4-DIHYDRONAPHTHALEN-1(2H)-ONE synthesis

3synthesis methods
Naphthalene, 6-bromo-1,1-difluoro-1,2,3,4-tetrahydro-

1415108-25-6
2 suppliers
inquiry

7-BROMO-4,4-DIFLUORO-3,4-DIHYDRONAPHTHALEN-1(2H)-ONE

1415108-26-7
19 suppliers
inquiry

-

Yield:1415108-26-7 71%

Reaction Conditions:

with potassium permanganate;potassium dihydrogenphosphate;trisodium phosphate*7H2O in water;tert-butyl alcohol at 20; for 15 h;

Steps:

c

c) 7-Bromo-4,4-difluoro-3,4-dihydro-2H-naphthalen-1-one A solution of 6-bromo-1,1-difluoro-1,2,3,4-tetrahydro-naphthalene (691 mg, 2.8 mmol) in tert-butanol (7 ml). A solution of potassium dihydrogenphosphate (769 mg, 5.59 mmol) in water (2 ml) and a solution of sodium phosphate heptahydrate (1.51 g, 5.59 mmol) in water (2 ml) were added. Thereafter, potassium permanganate (670 mg, 4.2 mmol) was added and the reaction mixture stirred at room temperature for 15 hours. For the workup, the mixture was diluted with ethyl acetate (200 ml), the organic layer separated, washed with water (10 ml) and brine (10 ml), finally dried over sodium sulphate and evaporated at reduced pressure. The crude product was purified by chromatography on silica gel using a gradient of heptane/ethyl acetate=100:0 to 80:20 as the eluent. The 7-bromo-4,4-difluoro-3,4-dihydro-2H-naphthalen-1-one (515 mg, 71% yield) was obtained as a colorless oil.

References:

US2012/302549,2012,A1 Location in patent:Page/Page column 30