反应详情

Into 170 ml of acetic acid, 11.0 g of ethyl 3-(4-chloro-2-nitrophenyl)-2-methyl-2-propenate were C) dissolved; and, while the mixture was stirred, 10.9 g (195.2 mmol) of iron powder (Koso Chem. Co.) and 13 ml of distilled water were added thereto at room temperature. The temperature of the mixture was raised, so that the reaction was carried out at 97° C. for 2 hours. After the end point of the reaction was verified by TLC, the reaction liquid was cooled, and acetic acid was evaporated under a reduced pressure. To the residue, 300 ml of water and 400 ml of ethyl acetate were added. Then, insoluble matters were filtered out. The filtrate was successively washed with water, an aqueous sodium hydrogencarbon ate solution, and a saturated aqueous sodium chloride solution; and then was dried for one night with sodium sulfate being added thereto. After sodium sulfate was filtered out, the filtrate was concentrated under a reduced pressure, whereby 9.8 g of a crude crystal were obtained. This crystal was refined by a silica gel column chromatography (aminopropyl-modified silica gel (Fuji Silysia Chem. Co., NH-DM1020); developing solvent: hexane/ethyl acetate=2/1), whereby 7.2 g of the aimed compound were obtained (yield: 73.3%).

1. dissolutiondissolved
2. customat room temperature
3. temperatureThe temperature of the mixture was raised, so that the reaction
4. customthe reaction liquid
5. temperaturewas cooled
6. customacetic acid was evaporated under a reduced pressure
7. additionTo the residue, 300 ml of water and 400 ml of ethyl acetate were added
8. filtrationThen, insoluble matters were filtered out
9. washThe filtrate was successively washed with water
10. dry with materialand then was dried for one night with sodium sulfate being
11. additionadded
12. filtrationAfter sodium sulfate was filtered out
13. concentrationthe filtrate was concentrated under a reduced pressure
14. customwhereby 9.8 g of a crude crystal were obtained