Lithium Chloride → (2-Bromophenyl)(tetrahydro-2H-pyran-4-yl)methanone

Lithium chloride (0.16 mL, 7.8 mmol) and copper cyanide (0.12 mL, 3.9 mmol) were dissolved in dry THF (4 mL) under nitrogen. This was added dropwise to pentamethylenebis(magnesium bromide) (0.5 M in THF, 7.79 mL, 3.9 mmol) in a dry ice bath under nitrogen and the mixture stirred for 30 min. I-Bromo-2-iodobenzene (0.50 mL, 3.9 mmol) was added and the flask was removed from the cold bath. After 30 min additional dry THF (5 mL) was added and stirred for another 40 min. Then tetrahydro-2H-pyran-4-carbonyl chloride (0.58 mL, 3.9 mmol) was added in one portion, and the mixture was stirred for 15 min. The reaction was quenched by addition of saturated ammonium chloride (10 mL). Ethyl acetate (100 mL) and water (100 mL) were added and the phases were mixed and separated. The organic layer was separated, dried with magnesium sulfate and evaporated to dryness under reduced pressure. Purification using silica column chromatography (hexane to ethyl acetate gradient) gave (2-bromophenyl)(tetrahydro-2H-pyran-4-yl)methanone as a thick oil.

1. customthe flask was removed from the cold bath
2. additionAfter 30 min additional dry THF (5 mL) was added
3. stirringstirred for another 40 min
4. stirringthe mixture was stirred for 15 min
5. customThe reaction was quenched by addition of saturated ammonium chloride (10 mL)
6. additionEthyl acetate (100 mL) and water (100 mL) were added
7. additionthe phases were mixed
8. customseparated
9. customThe organic layer was separated
10. dry with materialdried with magnesium sulfate
11. customevaporated to dryness under reduced pressure
12. customPurification

ORD record

ord-dff836534f2b4667bc15b944c9965aa3

Source dataset

uspto-grants-2014_05

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08735384B2