Hydrochloric Acid → HCID 178419182, compound

Under a nitrogen stream, a solution of cerium chloride (19.84 g, 2.98 equivalents) in THF (160 mL) was stirred at room temperature (25° C.) for 30 min. Sodium borohydride (3.11 g, 3.04 equivalents) was added, and the mixture was stirred at room temperature for 1.5 hrs. Then bis(p-tert-butylphenyl)phosphine oxide (8.49 g, 27.0 mmol) synthesized in Reference Example 15 and lithium aluminum hydride (1.55 g, 1.21 equivalents) were successively added at −17° C. and the mixture was stirred at room temperature for 2 hrs. Toluene (80 mL) was added at −10° C. and then 6M-HCl (25 mL) was added and water (25 mL) was added at 4° C. The mixture was stirred at room temperature for 30 min. The reaction mixture was partitioned, and the organic layer was washed successively with water (30 mL), 10% aqueous NaHCO3 solution (30 mL) and 10% aqueous NaCl solution (30 mL). The organic layer was dried over anhydrous magnesium sulfate, filtered by gravity, and further passed through a membrane filter (0.2 μm) under reduced pressure. The filtrate was concentrated under reduced pressure. The residue was dissolved in THF (100 mL) and a borane-THF complex (10 mL, 0.38 equivalent) was added at room temperature. The mixture was stirred for 16 hrs. and concentrated under reduced pressure. Toluene (30 mL) was added to the residue for dissolution, and the mixture was purified by silica gel column chromatography (silica gel 100 g, toluene), an effective fraction was concentrated under reduced pressure. The residue was recrystallized from n-hexane and dried (reduced pressure, 40° C.) to give the title compound (6.33 g, white powder). yield 75.0%. melting point: 151.5° C.

1. additionwere successively added at −17° C.
2. stirringthe mixture was stirred at room temperature for 2 hrs
3. stirringThe mixture was stirred at room temperature for 30 min
4. customThe reaction mixture was partitioned
5. washthe organic layer was washed successively with water (30 mL), 10% aqueous NaHCO3 solution (30 mL) and 10% aqueous NaCl solution (30 mL)
6. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
7. filtrationfiltered by gravity
8. filtrationfilter (0.2 μm) under reduced pressure
9. concentrationThe filtrate was concentrated under reduced pressure
10. dissolutionThe residue was dissolved in THF (100 mL)
11. additiona borane-THF complex (10 mL, 0.38 equivalent) was added at room temperature
12. stirringThe mixture was stirred for 16 hrs
13. concentrationand concentrated under reduced pressure
14. additionToluene (30 mL) was added to the residue for dissolution
15. customthe mixture was purified by silica gel column chromatography (silica gel 100 g, toluene)
16. concentrationan effective fraction was concentrated under reduced pressure
17. customThe residue was recrystallized from n-hexane
18. customdried (reduced pressure, 40° C.)

ORD record

ord-1b2b4c5e29ad45c2a706d7b8fe994d7c

Source dataset

uspto-grants-2011_11

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08053604B2