Dimethylformamide → 2-(4-bromophenyl)-N-methylacetamide

To a solution of 4-bromophenyl acetic acid (50 g, 233 mmol) in SOCl2 (170 mL, 2.32 mol) was added DMF (2 mL, 26 mmol). After stirred at this temperature for 1 h, the excess SOCl2 was removed under reduced pressure. The residue was dissolved in CH2Cl2 (300 mL), and the resulting solution was added to a cooled (0° C.) solution of CH3NH2 (90 mL, 40 wt % in H2O, 1.03 mol) in THF (200 mL) dropwise. After the addition was complete, the solution was further stirred at 0° C. for 15 min. Water (400 mL) was added to the reaction solution, and organic layer separated. The aqueous layer was extracted with CH2Cl2 (200 mL). The organic layers were combined, washed with brine (500 mL), dried and concentrated to give 4-bromophenyl-N-methyl acetamide (54 g, quant.) as a white solid: 1H NMR (500 MHz, CDCl3) δ 7.48 (d, J=8.9 Hz, 2H), 7.15 (d, J=8.9 Hz, 2H), 3.51 (s, 2H), 2.77 (s, 3H); ESI-MS m/z 228 [M+H]+.

1. customthe excess SOCl2 was removed under reduced pressure
2. dissolutionThe residue was dissolved in CH2Cl2 (300 mL)
3. additionthe resulting solution was added to
4. additionAfter the addition
5. stirringthe solution was further stirred at 0° C. for 15 min
6. customseparated
7. extractionThe aqueous layer was extracted with CH2Cl2 (200 mL)
8. washwashed with brine (500 mL)
9. customdried
10. concentrationconcentrated

ORD record

ord-9376a4e66f614853843f01307c827f45

Source dataset

uspto-grants-2014_06

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08741901B2