Dimethylformamide → 4-(Difluoromethyl)-2-fluorobenzaldehyde

Temperature

-78 °C

To a solution of 1-bromo-4-(difluoromethyl)-2-fluorobenzene (311 mg, 1.382 mmol) in THF (2.99 mL) was added butyllithium (1.6M solution in hexanes; 0.881 mL, 1.410 mmol) over ˜5 min at −78° C. The reaction mixture was stirred for 30 min at −78° C. then DMF (0.161 mL, 2.073 mmol) was added dropwise over ˜1 min. Stirring was continued for 20 min. The reaction mixture was quenched with aqueous 1M HCl solution/MeOH (2:1, 3 mL) and allowed to warm to room temperature. The mixture was diluted with 5 mL of water. The separated aqueous layer was with ether (5 mL). The combined organic layers were washed with 1M aqueous NaOH solution (10 mL) and saturated brine (10 mL), dried over MgSO4, filtered off and concentrated under reduced pressure. Repeated reaction with 420 mg of 1-bromo-4-(difluoromethyl)-2-fluorobenzene and combined crude materials for purification. The crude material was purified by column chromatography [SiO2, 24 g, heptane/ethyl acetate], providing 4-(difluoromethyl)-2-fluorobenzaldehyde (162.8 mg) as a yellow oil.

1. stirringStirring
2. waitwas continued for 20 min
3. customThe reaction mixture was quenched with aqueous 1M HCl solution/MeOH (2:1, 3 mL)
4. temperatureto warm to room temperature
5. additionThe mixture was diluted with 5 mL of water
6. washThe combined organic layers were washed with 1M aqueous NaOH solution (10 mL) and saturated brine (10 mL)
7. dry with materialdried over MgSO4
8. filtrationfiltered off
9. concentrationconcentrated under reduced pressure
10. customreaction with 420 mg of 1-bromo-4-(difluoromethyl)-2-fluorobenzene and combined crude materials
11. customfor purification
12. customThe crude material was purified by column chromatography [SiO2, 24 g, heptane/ethyl acetate]

ORD record

ord-7fd3fc38fec3470c9bccc93fb236d118

Source dataset

uspto-grants-2015_02

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08957068B2