4-Toluenesulfonyl chloride → 2,5-Difluoro-3-methoxyphenylacetonitrile

To a stirred solution of 2,5-difluoro-3-methoxybenzyl alcohol (8.26 g, 47.4 mmol) in dichloromethane (100 ml) was added p-toluenesulfonyl chloride (9.95 g, 52.2 mmol) and triethylamine (7.30 ml, 52.2 mmol) at room temperature. After 3.5 hr, the mixture was poured into water (200 ml) and extracted with ether (200 ml). The extract was washed with brine (200 ml), dried (magnesium sulfate) and evaporated. To the residue was added DMSO (200 ml) and sodium cyanide (3.48 g, 71 mmol). The resulting mixture was stirred for 2 hr and then poured into water (200 ml) and extracted with ether (300 ml). The extract was washed with water (100 ml), brine (100 ml) and dried over magnesium sulfate. Removal of solvent gave 5.91 g (63%) of the titled compound as a red oil.

1. extractionextracted with ether (200 ml)
2. washThe extract was washed with brine (200 ml)
3. dry with materialdried (magnesium sulfate)
4. customevaporated
5. extractionextracted with ether (300 ml)
6. washThe extract was washed with water (100 ml), brine (100 ml)
7. dry with materialdried over magnesium sulfate
8. customRemoval of solvent

ORD record

ord-eb8491a188fe43cd95e764be17c905ab

Source dataset

uspto-grants-2000_05

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US06063928