Reaktion #344452

Reaktionsgleichung

potassium carbonate

toluene

1-decene

sodium sulfite

→

decane 1,2-diol

Ausbeute 83.2%

Lösungsmittel

tert-butyl alcohol water

Ethyl acetate

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.STIRRINGthe mixture was stirred for an additional hour
2. 2
   Temperaturwarmed up to room temperature
3. 3
   Extraktionwas extracted with ethyl acetate (3×5 mL)
4. 4
   TrocknenCombined organic layer was dried over anhydrous magnesium sulfate
5. 5
   Einengenconcentrated in vacuo
6. 6
   SonstigeCrude product was purified by flash chromatography (silica gel, hexanes/EtOAc)

Vorschrift

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.

Quelle