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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 427231Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/427231

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2,6-HexanetriolHCID 7823—
EduktBenzaldehyde dimethyl acetalHCID 62375—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
Produkt1,3-Dioxolane-4-butanol, 2-phenyl-HCID 23668066,3%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

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 title 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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06312894B1
Quelldatensatzuspto-grants-2001_11
ORD IDord-f144324ce65f439cb729c903d2fc236e
Quellennotizuspto-grants-2001_11