反应详情

Under a nitrogen atmosphere, alpha-(4-picolylthio) acetophenone (852 mg., 3.5 mmoles) was dissolved in 8.75 ml. of isopropyl alcohol. Sodium borohydride (54 mg., 1.4 mmoles, 1.6 equiv.) was added. After stirring for 0.5 hour at room temperature, the reaction mixture was refluxed for 1 hour. The reaction mixture was cooled somewhat and then evaporated to an oil. With stirring, hydrochloric acid (4N, 10 ml.) was added slowly to the oil, so as to control heating and foaming. Once addition was complete and there was no evidence of gas evolution, the acid solution was made strongly basic with 20% sodium hydroxide. The oil which precipitated was extracted into chloroform. The chloroform was back-washed with dilute sodium hydroxide, dried over anhydrous sodium sulfate and concentrated to an oil (0.87 g.) which crystallized to a waxy solid on standing. The solid was triturated with ether and filtered to yield crude product (0.61 g.). Recrystallization from ethyl acetate gave purified 4-(2-hydroxy-2-phenylethylthiomethyl)pyridine [0.42 g.; m.p. 116.5°-119° C. (incomplete); ir (KBr): 3.17, 5.1-5.8, 6.22, 6.88, 9.49, 12.25, 13.88 and 14.25μ; mass spectra: m/e calcd.: 245, found: 245; pnmr/CDCl3 /TMS/delta: 8.73-8.37 (m, 2H), 7.57-7.10 (m, 7H), 4.75 (t, 1H), 3.63 (s, 2H), 3.10 (s, 1H, exchanges with D2O) and 2.72 (d, 2H)].

1. temperaturethe reaction mixture was refluxed for 1 hour
2. temperatureThe reaction mixture was cooled somewhat
3. customevaporated to an oil
4. stirringWith stirring
5. additionhydrochloric acid (4N, 10 ml.) was added slowly to the oil
6. temperatureso as to control heating
7. additionOnce addition
8. customThe oil which precipitated
9. extractionwas extracted into chloroform
10. washThe chloroform was back-washed with dilute sodium hydroxide
11. dry with materialdried over anhydrous sodium sulfate
12. concentrationconcentrated to an oil (0.87 g.) which
13. customcrystallized to a waxy solid
14. customThe solid was triturated with ether
15. filtrationfiltered