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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1285069생성일: 2026년 10월 26일

Methoxymethyl-triphenylphosphonium chloride → HCID 178495003, 화합물

https://huagongshe.com/reaction/1285069

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참여 물질

역할이름HCID투입량
반응물Methoxymethyl-triphenylphosphonium chlorideHCID 2723798—
반응물HCID 178509798HCID 178509798—
용매TetrahydrofuranHCID 8028—
용매tert-Butyl methyl etherHCID 15413—
생성물HCID 178495003HCID 17849500396%

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온도0 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04565425
출처 데이터셋uspto-grants-1986_01
ORD IDord-b39d169891704f8f8456092b043d2ce1
출처 메모uspto-grants-1986_01