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HRID 975742作成日:2026年10月27日

Tetrahydrofuran → 4-(4-Propylcyclohexyl)cyclohexane

https://huagongshe.com/reaction/975742

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物Phosphine, triphenyl-, hydrobromideHCID 517696—
反応物[1,1'-Bicyclohexyl]-4-one,4'-propyl-,HCID 4354185—
反応物Potassium tert-butoxideHCID 23665647—
溶媒Diethyl EtherHCID 3283—
生成物4-(4-Propylcyclohexyl)cyclohexaneHCID 1788409756%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05609791
出典データセットuspto-grants-1997_03
ORD IDord-b6001f375b1c4dde9bc2c80ccc1b1963
出典メモuspto-grants-1997_03