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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 975742생성일: 2026년 10월 26일

Tetrahydrofuran → 4-(4-Propylcyclohexyl)cyclohexane

https://huagongshe.com/reaction/975742

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물Phosphine, triphenyl-, hydrobromideHCID 517696—
반응물[1,1'-Bicyclohexyl]-4-one,4'-propyl-,HCID 4354185—
반응물Potassium tert-butoxideHCID 23665647—
용매Diethyl EtherHCID 3283—
생성물4-(4-Propylcyclohexyl)cyclohexaneHCID 1788409756%

반응 단계

Into a three-necked flask equipped with a dropping funnel, a three-way cock and a thermometer was placed (2-(1,3-dioxan)-2-yl)ethyl)triphenylphosphonium bromide (12.3 g, 27 mmols), followed by adding tetrahydrofuran (50 ml), suspending, stirring under ice cooling till the liquid temperature reached 10° C. The reaction mixture is added potassium t-butoxide (3.0 g, 27 mmols), followed by elevating the temperature up to room temperature under ice cooling for one hour, stirring for one hour, dropwise adding a tetrahydrofuran (10 ml) solution of 4-(4-propylcyclohexyl)cyclohexanone (15.6 g, 25 mmols) over 30 minutes from the dropping funnel, further stirring the reaction mixture for 5 hours after completion of the dropwise addition, adding ether (50 ml), allowing to stand for one hour, filtering off deposited insoluble substance, concentrating the filtrate under reduced pressure, isolating and purifying the resulting pale brown oily substance by means of silica gel column chromatography and recrystallizing from ethanol, to obtain 1-(2-(1,3-dioxan)-2-yl)ethylidene)-4-(4-propylcyclohexyl)cyclohexane (4.5 g, 14 mmols).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05609791
출처 데이터셋uspto-grants-1997_03
ORD IDord-b6001f375b1c4dde9bc2c80ccc1b1963
출처 메모uspto-grants-1997_03