Hydrochloric Acid → HCID 18357338, compound

A mixture of 6-(2-hydroxy-ethyl)-4-phenyl-chroman-2-ol (Example 7, 30 g, 111 mmol, 1 equiv), diisopropylamine (33.7 g, 333 mmol, 3 eq) and palladium hydroxide on carbon [50% wet catalyst (50% by weight is water), 6 g, 0.2 equiv] in toluene (120 mL) was hydrogenated at 621×103 Nm−2 (90 psi) hydrogen pressure at 110° C. The reaction mixture was cooled to room temperature and filtered through arbocel and evaporated under reduced pressure. The resulting oil was dissolved in acetonitrile (200 mL) and concentrated hydrochloric acid (11.6 mL, 1.05 equiv) was added. The mixture was distilled at ambient pressure, removing approximately 100 mL of acetonitrile, and the distilled solvent replaced with fresh acetonitrile. The mixture was allowed to cool and crystallise overnight. The product was filtered and washed with a small portion of acetonitrile and dried overnight in vacuo at 50° C. to give the title compounds as a white solid (26.7 g, 68.1 mmol, 61%).

1. filtrationfiltered through arbocel
2. customevaporated under reduced pressure
3. dissolutionThe resulting oil was dissolved in acetonitrile (200 mL)
4. distillationThe mixture was distilled at ambient pressure
5. customremoving approximately 100 mL of acetonitrile
6. temperatureto cool
7. customcrystallise overnight
8. filtrationThe product was filtered
9. washwashed with a small portion of acetonitrile
10. customdried overnight in vacuo at 50° C.

ORD record

ord-732f3b33d03c4e66b04b4a31767e0a71

Source dataset

uspto-grants-2011_11

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08067594B2