反应详情

To the mixture of 0.2 g of lithium aluminum hydride and 20 ml of anhydrous tetrahydrofuran was added with stirring under ice-cooling 400 mg of 2-trifluoromethyl-9-chloro-11-chloro-10,11-dihydrodibenzo[b,f]thiepin dissolved in 10 ml of anhydrous tetrahydrofuran. Thereafter, the mixture was reacted under cooling for 0.5 hr. at the room temperature and further under reflux condition for 3.5 hrs. After cooling, to the mixture was added water with stirring under cooling to decompose an excess of lithium aluminum hydroxide and the resulting mixture was filtered with the use of celite. The filtrate was extracted with chloroform, chloroform layer was washed with water and dried over anhydrous sodium sulfate. The solvent was evaporated to obtain 372 ml of an oily substance, which was chromatographed on a silica gel, eluted with n-hexane, and there was obtained 65 mg of 2-trifluoromethyl-9-chloro-10,11-dihydrodibenzo[b,f]thiepin.

1. additionwas added
2. customThereafter, the mixture was reacted
3. temperatureunder cooling for 0.5 hr
4. temperatureAfter cooling, to the mixture
5. stirringwith stirring
6. temperatureunder cooling
7. filtrationthe resulting mixture was filtered with the use of celite
8. extractionThe filtrate was extracted with chloroform, chloroform layer
9. washwas washed with water
10. dry with materialdried over anhydrous sodium sulfate
11. customThe solvent was evaporated
12. customto obtain 372 ml of an oily substance, which
13. customwas chromatographed on a silica gel
14. washeluted with n-hexane