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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 257270Generated: October 26, 2026

Toluene → 1,2-Decanediol

https://huagongshe.com/reaction/257270

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPotassium CarbonateHCID 11430—
Reactant1-DeceneHCID 13381—
ReactantSodium SulfiteHCID 24437—
CatalystOsmium TetroxideHCID 30318—
CatalystHCID 178511488HCID 178511488—
SolventEthyl AcetateHCID 8857—
Solvent2-Methylpropan-2-ol--water (1/1)HCID 71401949—
Product1,2-DecanediolHCID 7914183.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05260461
Source datasetuspto-grants-1993_11
ORD IDord-5d317fd0c8aa4f019316bfb9a8cfe508
Source noteuspto-grants-1993_11