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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 39707생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Citric AcidHCID 311—
반응물DiisopropylamineHCID 7912—
반응물Benzene, ((2-bromoethoxy)methyl)-HCID 73833—
반응물1,4-Dioxaspiro[4.5]decane-8-carbonitrileHCID 11116433—
반응물HCID 178418244HCID 178418244—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물8-(2-(Benzyloxy)ethyl)-1,4-dioxaspiro[4.5]decane-8-carbonitrileHCID 67539292—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524738B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-d5b6baf518b046cfb7ba5027910852b9
출처 메모uspto-grants-2013_09