Methane, dichloromethoxy- → 2-Methoxy-5-(2,2,2-trifluoroethyl)benzaldehyde

To a stirred solution of Compound 45 (760 mg, 4.00 mmol) in dry CH2Cl2 (15 ml) was added TiCl4 (1.67 g, 8.80 mmol) via a syringe with ice-cooling. After 15 min, to this was added a solution of dichloromethyl methyl ether (920 mg, 8.00 mmol) in dry CH2Cl2 (5 ml) at same temperature. The reaction mixture was stirred at 0 C. for 15 min, and then for 1.5 h at room temperature. The mixture was diluted with water (20 ml) with ice-cooling and stirred at room temperature for 15 min. The organic layer was separated and the aqueous layer was extracted with CH2Cl2. The combined solution was washed with sat. NaHCO3 aq. and brine, dried (MgSO4), and concentrated in vacuo to give crude product as a yellow oil. The crude product was purified by column chromatography on silica gel with hexane-ethyl acetate (40:1-20:1) to give Compound 46 (500 mg, 57%) as a colorless solid(needle).

1. temperaturecooling
2. waitfor 15 min
3. waitfor 1.5 h at room temperature
4. temperaturecooling
5. stirringstirred at room temperature for 15 min
6. customThe organic layer was separated
7. extractionthe aqueous layer was extracted with CH2Cl2
8. washThe combined solution was washed with sat. NaHCO3 aq. and brine
9. dry with materialdried (MgSO4)
10. concentrationconcentrated in vacuo
11. customto give crude product as a yellow oil
12. customThe crude product was purified by column chromatography on silica gel with hexane-ethyl acetate (40:1-20:1)

ORD record

ord-a92170dec14940bc88f7dc681ca5944e

Source dataset

uspto-grants-2001_12

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US06329396B1