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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 257270Erstellt: 24. Oktober 2026

Toluene → 1,2-Decanediol

https://huagongshe.com/de/reaction/257270

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTolueneHCID 1140—
EduktPotassium CarbonateHCID 11430—
Edukt1-DeceneHCID 13381—
EduktSodium SulfiteHCID 24437—
KatalysatorOsmium TetroxideHCID 30318—
KatalysatorHCID 178511488HCID 178511488—
LösungsmittelEthyl AcetateHCID 8857—
Lösungsmittel2-Methylpropan-2-ol--water (1/1)HCID 71401949—
Produkt1,2-DecanediolHCID 7914183,2%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a well-stirred solution of bis-1,4-(9'-O-dihydroquinidine)phthalazine (7.8 mg, 0.01 mmol), potassium ferricyanide (0.99 g, 3 mmol), potassium carbonate (0.42 g, 3 mmol), and osmium tetroxide (0.1 mL of a 0.1M toluene solution, 0.01 mmol) in 15 mL of a tert-butyl alcohol-water (1:1, v/v) at 0° C., 1-decene (0.14 g, 0.19 mL, 1 mmol) was added in one portion. The mixture was stirred for 24 h at 0° C. Solid sodium sulfite (1.5 g) was added and the mixture was stirred for an additional hour, and then warmed up to room temperature. Ethyl acetate (10 mL) was added to the reaction mixture, and aqueous layer was extracted with ethyl acetate (3×5 mL). Combined organic layer was dried over anhydrous magnesium sulfate, and concentrated in vacuo. Crude product was purified by flash chromatography (silica gel, hexanes/EtOAc) to afford decane 1,2-diol as a white solid (0.145 g, 83%). HPLC analysis of the bis-Mosher ester of this crude decane 1,2 diol gave 84% ee.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05260461
Quelldatensatzuspto-grants-1993_11
ORD IDord-5d317fd0c8aa4f019316bfb9a8cfe508
Quellennotizuspto-grants-1993_11