1,2,6-Hexanetriol → 1,3-Dioxolane-4-butanol, 2-phenyl-

Temperatur

100 °C

To a solution of 1,2,6-trihydroxyhexane (10.0 g, 74.6 mmol) and benzaldehyde dimethylacetal (15.0 g, 98.7 mmol) in dry DMF (10 mL) was added Amberlyst 15 (5.0 g). The mixture was stirred at 100° C. for 5 min, then cooled and filtered. The filtrate was concentrated and residue obtained was re-dissolved in ethyl acetate. After being washed with water and brine, the solution was dried over Na2SO4. The crude product obtained after evaporation of the solvent was chromatographed on silica eluting with ethyl acetate. Concentration of the proper fractions afforded 11.0 g (66%) of the tide product (a mixture of diastereomers) as a colorless oil: 1H NMR (CDCl3, 300 MHz, ppm) 7.48 (m, 2H), 7.39 (m, 3H), 5.92 (s, 0.4H), 5.80 (s, 0.6H), 4.3-4.1 (m, 2H), 3.64 (m, 3H), 1.8-1.4 (m, 6H).

1. temperaturecooled
2. filtrationfiltered
3. concentrationThe filtrate was concentrated
4. customresidue obtained
5. washAfter being washed with water and brine
6. dry with materialthe solution was dried over Na2SO4
7. customThe crude product obtained
8. customafter evaporation of the solvent
9. customwas chromatographed on silica eluting with ethyl acetate

ORD-Eintrag

ord-3f4648cec5a649109e0f03d8cdef7429

Quelldatensatz

uspto-grants-2013_06

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US08465921B2