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HRID 257270作成日:2026年10月26日

Toluene → 1,2-Decanediol

https://huagongshe.com/reaction/257270

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物Potassium CarbonateHCID 11430—
反応物1-DeceneHCID 13381—
反応物Sodium SulfiteHCID 24437—
触媒Osmium TetroxideHCID 30318—
触媒HCID 178511488HCID 178511488—
溶媒Ethyl AcetateHCID 8857—
溶媒2-Methylpropan-2-ol--water (1/1)HCID 71401949—
生成物1,2-DecanediolHCID 7914183.2%

反応条件

温度0 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05260461
出典データセットuspto-grants-1993_11
ORD IDord-5d317fd0c8aa4f019316bfb9a8cfe508
出典メモuspto-grants-1993_11