反应详情

温度

35 °C

To a suspension of sodium borohydride (43.5 g) dispersed in THF (327 ml) was added trimethyl borate (9.1 g) and added dropwise at 20-30° C. a solution of 4-(4′-fluorobenzoyl)isophthalic acid (100.5 g) synthesized in Example 4 in THF (313 ml), and the mixture was heated to 35° C. A boron trifluoride-THF complex (181.7 g) was added dropwise at 35-42° C. After the dropwise addition, the mixture was heated at 40-50° C. for 7 hr, and hydrolyzed with water (101 ml) in an ice bath. THF was evaporated under reduced pressure. To the residue was added 30% sulfuric acid (110 g) and the mixture was stirred at 60° C. for 5 hr. A 25% aqueous solution of sodium hydroxide (200 g) was added and the mixture was extracted with hot toluene (450 ml) at 70° C. The hot toluene layer was washed with warm water (70° C., 60 ml), heptane (450 ml) was added and the mixture was cooled. The precipitated crystals were collected by filtration and dried to give 1-(4′-fluorophenyl)-1,3-dihydroisobenzofuran-5-ylmethanol (69.0 g, 81%). The various spectrum data of the crystals were the same as those obtained in Example 12.

1. additionA boron trifluoride-THF complex (181.7 g) was added dropwise at 35-42° C
2. additionAfter the dropwise addition
3. temperaturethe mixture was heated at 40-50° C. for 7 hr
4. customTHF was evaporated under reduced pressure
5. additionTo the residue was added 30% sulfuric acid (110 g)
6. additionA 25% aqueous solution of sodium hydroxide (200 g) was added
7. extractionthe mixture was extracted with hot toluene (450 ml) at 70° C
8. washThe hot toluene layer was washed with warm water (70° C., 60 ml), heptane (450 ml)
9. additionwas added
10. temperaturethe mixture was cooled
11. filtrationThe precipitated crystals were collected by filtration
12. customdried