对氯苯乙酮 → 1-[4-(4-Hydroxybutylsulfanyl)phenyl]ethanone

温度

110 °C

To a stirred solution of 4-hydroxybutanethiol (5.0 g, 47 mmol) in DMF (100 mL) was added NaH (60% dispersion in mineral oil 2.1 g). After the effervescence had ceased, p-chloroacetophenone (4.3 mL, 33 mmol) was added. The solution was then stirred at 110° C. for 3 h. The mixture was cooled to RT and then diluted with ether (200 mL). The ethereal suspension was washed with 5% HCl (aq, 2×100 mL), water (100 mL), and then brine (50 mL). The ether extract was dried (MgSO4), filtered and concentrated to afford crude 1-[4-(4-hydroxybutylsulfanyl)phenyl]ethanone, which was used without purification. 1-[4-(4-hydroxybutylsulfanyl)phenyl]ethanone was taken up in dimethylformamide dimethylacetal (100 mL) and stirred at reflux for 12 h. The mixture was cooled and then concentrated to about one half of the original volume. Hexane was added to precipitate 3-Dimethylamino-1-[4-(4-hydroxybutylsulfanyl)phenyl]propenone. The mixture was filtered, washed with hexanes (50 mL), and dried to afford 3-Dimethylamino-1-[4-(4-hydroxy-butylsulfanyl)phenyl]propenone (6.4 g, 23 mmol): HPLC Retention Time; 5.58 min. (Method B) M+1; 279.8.

1. temperatureThe mixture was cooled to RT
2. washThe ethereal suspension was washed with 5% HCl (aq, 2×100 mL), water (100 mL)
3. extractionThe ether extract
4. dry with materialwas dried (MgSO4)
5. filtrationfiltered
6. concentrationconcentrated

ORD记录

ord-ea712a3326f642599e5b94029e696014

来源数据集

uspto-grants-2008_09

DOI

10.6084/m9.figshare.5104873.v1

专利号

US07429599B2