2-Butenamide, N-(4-bromophenyl)-3-methyl- → 6-bromo-4,4-dimethyl-3,4-dihydroquinolin-2(1H)-one

温度

130 °C

To 6.7 g (26.02 mmol) of molten N-(4-bromophenyl)3,3-dimethylacrylamide (Compound 92) (heated to 135 degrees C.) was added 4.15 g (31.09) of aluminum chloride over 25 min. The reaction mixture was stirred at 130 degrees C. for 16 h and then treated with a further 1 g (7.5 mmol) of aluminum chloride. The reaction mixture was heated at 130 degrees C for a further 9 h and then cooled to room temperature: The reaction was then quenched by the slow addition of 100 ml of ice cold water with slight warming of flask to facilitate mixing. The mixture was extracted with 1×100 ml and 4×50 ml of ether. The organic extracts were combined and washed with 25 ml of saturated NaCl solution and then dried (MgSO4). The solvent was removed in vacuo and the residue purified by flash chromatography (silica; 30% ethyl acetate in hexanes) to give the title compound as a pale yellow solid. PMR (CDCl3): δ 1.37 (6H, s), 2.53 (2H, s), 6.85 (1H, d, J~8.4 Hz), 7.32 (1H, dd, J~8.4 Hz, 2.1 Hz), 7.43 (1H, d, J~2.81 Hz), 10.12 (1H, broad s).

1. temperatureThe reaction mixture was heated at 130 degrees C for a further 9 h
2. temperaturecooled to room temperature
3. customThe reaction was then quenched by the slow addition of 100 ml of ice cold water
4. temperaturewith slight warming of flask
5. additionto facilitate mixing
6. extractionThe mixture was extracted with 1×100 ml and 4×50 ml of ether
7. washwashed with 25 ml of saturated NaCl solution
8. dry with materialdried (MgSO4)
9. customThe solvent was removed in vacuo
10. customthe residue purified by flash chromatography (silica; 30% ethyl acetate in hexanes)

ORDレコード

ord-6cb26ad1fba64b678a6b1a50558d49a1

出典データセット

uspto-grants-1993_09

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US05248777