反应详情

温度

-40 °C

To methyl 3-(4-methylbenzyloxy)-5-oxo-6,7,8,9-tetrahydro-5H-benzocycloheptene-6-carboxylate (2.77 g, 8.19 mmol) dissolved in a mixed solvent of dichloromethane (40 ml) and methanol (10 ml) was added at −40° C. (inner temperature) sodium borohydride (465 mg, 12.3 mmol), and the resulting mixture was stirred at −20° C. to −10° C. for 2 hours. The reaction mixture was cooled to −40° C., was mixed with water (20 ml) and extracted with dichloromethane (40 ml, 10 ml×2). The combined organic layers were dried with anhydrous magnesium sulfate and were then concentrated under reduced pressure. To the residue dissolved in THF (30 ml) were added at 0° C. triethylamine (5.70 ml, 40.9 mmol) and methanesulfonyl chloride (0.95 ml, 12.3 mmol), and the resulting mixture was stirred at room temperature for 12 hours. In order to complete the reaction, DBU (3.67 ml, 24.5 mmol) and dichloromethane (30 ml) were added, and the resulting mixture was stirred at room temperature for 3 hours. The reaction mixture was concentrated under reduced pressure, was mixed with water (30 ml) and was extracted with ethyl acetate (30 ml×3). The combined organic layers were washed with 1 N hydrochloric acid (5 ml×3), were dried with anhydrous magnesium sulfate and were then concentrated under reduced pressure, and the residue was subjected to column chromatography (silica gel: 60 g, ethyl acetate/hexane=1/30→1/9). The objective fractions were concentrated under reduced pressure to obtain methyl 2-(4-methylbenzyloxy)-6,7-dihydro-5H-benzocycloheptene-8-carboxylate (2.40 g, 7.44 mmol, 91%).

1. extractionextracted with dichloromethane (40 ml, 10 ml×2)
2. dry with materialThe combined organic layers were dried with anhydrous magnesium sulfate
3. concentrationwere then concentrated under reduced pressure
4. dissolutionTo the residue dissolved in THF (30 ml)
5. stirringthe resulting mixture was stirred at room temperature for 12 hours
6. additionwere added
7. stirringthe resulting mixture was stirred at room temperature for 3 hours
8. concentrationThe reaction mixture was concentrated under reduced pressure
9. additionwas mixed with water (30 ml)
10. extractionwas extracted with ethyl acetate (30 ml×3)
11. washThe combined organic layers were washed with 1 N hydrochloric acid (5 ml×3)
12. dry with materialwere dried with anhydrous magnesium sulfate
13. concentrationwere then concentrated under reduced pressure
14. concentrationThe objective fractions were concentrated under reduced pressure