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HRID 39707作成日:2026年10月24日

Citric Acid → 8-(2-(Benzyloxy)ethyl)-1,4-dioxaspiro[4.5]decane-8-carbonitrile

https://huagongshe.com/ja/reaction/39707

反応式

関与物質

役割名称HCID仕込み量
反応物Citric AcidHCID 311—
反応物DiisopropylamineHCID 7912—
反応物Benzene, ((2-bromoethoxy)methyl)-HCID 73833—
反応物1,4-Dioxaspiro[4.5]decane-8-carbonitrileHCID 11116433—
反応物HCID 178418244HCID 178418244—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物8-(2-(Benzyloxy)ethyl)-1,4-dioxaspiro[4.5]decane-8-carbonitrileHCID 67539292—

反応手順

To 8 mL of a tetrahydrofuran solution containing 0.94 mL of diisopropylamine, 4.5 mL of 1.6 mol/L butyllithium/hexane was added dropwise at −78° C., the mixture was stirred at the same temperature for 1 hour, and then thereto was added dropwise 7 mL of a tetrahydrofuran solution containing 0.60 g of 1,4-dioxaspiro[4.5]decane-8-carbonitrile. After stirring at −78° C. for 1 hour, the mixture was added dropwise with 0.85 mL of benzyl 2-bromoethyl ether, and further stirred for 1 hour. The temperature of the reaction mixture was increased to room temperature, and then a 10% aqueous citric acid solution and ethyl acetate were added thereto. The organic layer was separated, and the aqueous layer was extracted with ethyl acetate. The organic layer and the extract were combined, the resultant solution was washed with an aqueous saturated sodium chloride solution and then dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residue thus obtained was purified by silica gel column chromatography [eluent; hexane:ethyl acetate=6:1] to obtain 1.1 g of a colorless oily substance, 8-(2-(benzyloxy)ethyl)-1,4-dioxaspiro[4.5]decane-8-carbonitrile.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524738B2
出典データセットuspto-grants-2013_09
ORD IDord-d5b6baf518b046cfb7ba5027910852b9
出典メモuspto-grants-2013_09