Dimethylformamide → N,N-diethyl-4-formylbenzamide

4-Carboxybenzaldehyde (100.3 g, 0.67 mol) was dissolved/suspended in toluene (1200 mL), N, N-dimethylformamide (0.15 mL) was added and the suspension was stirred during the dropwise addition of thionyl chloride (53.5 mL, 87.2 g, 0.73 mol). The reaction mixture was heated to reflux under nitrogen and stirred for 2 hours, during which time most, but not all, of the aldehydo-acid passed into solution. A further quantity of thionyl chloride (20 mL, 32.6 g, 0.27 mol) was added and reflux continued overnight. The clear reaction mixture was evaporated, and the residue dissolved in anhydrous tetrahydrofuran (1500 mL). The solution was cooled in an ice/water bath and diethylamine (173 mL, 122 g, 1.67 mol (2.5 equivalents)) was added dropwise to the stirred solution. The ice-bath was removed and stirring continued for 2.5 h. The reaction mixture was filtered to remove the white crystalline diethylamine hydrochloride by-product. The crystals were washed with ethyl acetate (2×600 mL), and the washings set aside. The tetrahydrofuran filtrate was evaporated, and the residue dissolved in the ethyl acetate washings. The solution was washed sequentially with 1 M hydrochloric acid (2×600 mL), water (2×300 mL), dilute sodium carbonate solution (saturated: H2O/1:1, 2×600 mL), water (2×300 mL) and saturated sodium chloride solution (300 mL). The organic layer was separated, dried over anhydrous sodium sulfate and evaporated to yield 4-formyl-N, N-diethylbenzamide as a pale brown oil, which was used without further purification. (Yield: 115.7 g, 84%).

1. temperatureThe reaction mixture was heated
2. temperatureto reflux under nitrogen
3. temperaturereflux
4. waitcontinued overnight
5. customThe clear reaction mixture was evaporated
6. dissolutionthe residue dissolved in anhydrous tetrahydrofuran (1500 mL)
7. temperatureThe solution was cooled in an ice/water bath
8. customThe ice-bath was removed
9. stirringstirring
10. waitcontinued for 2.5 h
11. filtrationThe reaction mixture was filtered
12. customto remove the white crystalline diethylamine hydrochloride by-product
13. washThe crystals were washed with ethyl acetate (2×600 mL)
14. customThe tetrahydrofuran filtrate was evaporated
15. dissolutionthe residue dissolved in the ethyl acetate washings
16. washThe solution was washed sequentially with 1 M hydrochloric acid (2×600 mL), water (2×300 mL), dilute sodium carbonate solution (saturated: H2O/1:1, 2×600 mL), water (2×300 mL) and saturated sodium chloride solution (300 mL)
17. customThe organic layer was separated
18. dry with materialdried over anhydrous sodium sulfate
19. customevaporated

ORD record

ord-f6f5fb444ceb40f0a23347ab5df7685d

Source dataset

uspto-grants-2008_01

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07314880B2