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HRID 2050467作成日:2026年10月25日

Methoxymethyl-triphenylphosphonium chloride → HCID 178495003、化合物

https://huagongshe.com/reaction/2050467

反応式

関与物質

役割名称HCID仕込み量
反応物Methoxymethyl-triphenylphosphonium chlorideHCID 2723798—
反応物HCID 178509798HCID 178509798—
溶媒TetrahydrofuranHCID 8028—
溶媒tert-Butyl methyl etherHCID 15413—
生成物HCID 178495003HCID 17849500396%

反応条件

温度0 °C

反応手順

A suspension of 22.2 g of methoxymethyl-triphenylphosphonium chloride in 150 ml of t-butyl methyl ether was treated with 7.4 g of solid potassium t-butylate at 0° C. within 3 minutes while gassing with argon in a sulphonation flask provided with a mechanical stirrer. The orange suspension was stirred at 0° C. for 1 hour and then treated dropwise within 10 minutes with a solution of 9.8 g of 2-[trans-4-(p-cyanophenyl)cyclohexyl]acetaldehyde in 100 ml of tetrahydrofuran. Subsequently, the suspension was left to warm slowly to room temperature while stirring. After 15 hours, the suspension was partitioned three times in diethyl ether/water. The organic extracts were washed twice with water, dried over magnesium sulphate, filtered and evaporated. In order to separate triphenylphosphine oxide, the residue was dissolved in ethyl acetate and the solution was diluted with petroleum ether, filtered and evaporated. Chromatographic separation of the resulting, yellowish oil (13.7 g) on silica gel with ethyl acetate/petroleum ether (vol. 5:95) gave 10.5 g (96%) of p-[trans-4-(3-methoxy-2-propenyl)cyclohexyl]benzonitrile as a colourless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05013478
出典データセットuspto-grants-1991_05
ORD IDord-14383572e0264dc9b7e583de2e9802fb
出典メモuspto-grants-1991_05