4-Methylbenzoyl Chloride → Oxo-P-tolyl-acetonitrile

p-Toluoyl cyanide was prepared according to the general procedure reported by Olah et al. [supra]. Under dry conditions, 1.35 mL of p-toluoyl chloride (98%, Aldrich) (10.2 mmol), 26 mL of methylene chloride, freshly distilled from phosphorus pentoxide under nitrogen, and 1.53 mL of trimethylsilyl cyanide (11.5 mmol) were added to a 100-mL round bottom flask. To this solution 0.25 mL of tin (IV) chloride (2.1 mmol) was added. This mixture was stirred for 2 hr at room temperature. During the 2 hr, the color of the solution changed from pale yellow to dark brown. After 2 hr the reaction mixture was quenched with 75 mL of ice-cold water and then extracted with two 75-mL portions of methylene chloride. The methylene chloride extracts were combined, washed with two 75-mL portions of ice-cold water, dried with MgSO4, and filtered. The methylene chloride was removed by rotary evaporation to yield a dark brown oil which solidifed on standing. This crude product was dissolved in hexanes and filtered. The solvent was removed by rotary evaporation to yield 1.266 g (86%) of p-toluoyl cyanide as a yellow solid: IR (CCl4) (partial) 2220, 1685, 1607 cm-1.

1. customp-Toluoyl cyanide was prepared
2. customDuring the 2 hr
3. customAfter 2 hr the reaction mixture was quenched with 75 mL of ice-cold water
4. extractionextracted with two 75-mL portions of methylene chloride
5. washwashed with two 75-mL portions of ice-cold water
6. dry with materialdried with MgSO4
7. filtrationfiltered
8. customThe methylene chloride was removed by rotary evaporation
9. customto yield a dark brown oil which
10. filtrationfiltered
11. customThe solvent was removed by rotary evaporation

ORD record

ord-cb45ddc895c24cdd87d51d4f67d6145c

Source dataset

uspto-grants-1990_07

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US04942247