Benzene, 4-chloro-1-methyl-2-nitro- → 4-Chloro-2-nitrobenzaldehyde

A solution of 4-chloro-2-nitrotoluene (514.8 mg, 3.000 mmol) and dimethylformamide dimethylacetal (1.200 ml, 1074 mg, 9.000 mmol) in DMF (1.2 ml) was heated at 135° C. in a sealed tube for 15 h. The reaction mixture was cooled to rt and added dropwise to a 20° C. solution of NaIO4 (1926 mg, 9.000 mmol) in water (6.18 ml) and DMF (3.09 ml). After 3 h, the mixture was treated with water (20 ml) and extracted with EtOAc (3×15 ml). The extracts were washed with water (3×15 ml) and brine (15 ml), and dried over MgSO4. After the solid was filtered off and the solvent was removed in vacuo, a brown solid of 4-chloro-2-nitrobenzaldehyde was obtained (J. Org. Chem. 2003, 68, 4104-4107). NMR (CDCl3, 400 MHz) δ 7.74-7.78 (m, 1 H), 7.94-7.96 (m, 1 H), 8.11-8.12 (m, 1 H), 10.39 (s, 1 H).

1. extractionextracted with EtOAc (3×15 ml)
2. washThe extracts were washed with water (3×15 ml) and brine (15 ml)
3. dry with materialdried over MgSO4
4. filtrationAfter the solid was filtered off
5. customthe solvent was removed in vacuo

ORD-Eintrag

ord-ab2e214c35004202adcaa830656244ec

Quelldatensatz

uspto-grants-2013_02

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US08367826B2