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HRID 1285070作成日:2026年10月25日

tert-Butyl methyl ether → HCID 178444326、化合物

https://huagongshe.com/reaction/1285070

反応式

関与物質

役割名称HCID仕込み量
反応物tert-Butyl methyl etherHCID 15413—
反応物HCID 178509797HCID 178509797—
触媒Phosphonium, ethyltriphenyl-, bromide (1:1)HCID 73727—
生成物HCID 178444326HCID 17844432689%

反応手順

A suspension of 14.8 g of ethyltriphenylphosphonium bromide in 150 ml of t-butyl methyl ether was treated with 4.54 g of solid potassium t-butylate at -10° C. within 5 minutes while gassing with argon in a sulphonation flask provided with a mechanical stirrer. The suspension was stirred at room temperature for 1 hour, then treated dropwise at 0° C. within 5 minutes with a solution of 6.4 g of 3-[trans-4-(p-cyanophenyl)cyclohexyl]propionaldehyde in 40 ml of t-butyl methyl ether and stirred at room temperature for a further 15 hours. The mixture was subsequently partitioned three times in diethyl ether/water. The organic extracts were washed twice with water, dried over magnesium sulphate, filtered and concentrated. In order to separate triphenylphosphine oxide, the residue was dissolved in ethyl acetate and the solution was diluted with petroleum ether, filtered and concentrated. Chromatographic separation of the resulting, yellowish oil (8.55 g) on silica gel with ethyl acetate/petroleum ether (vol. 3:97) gave 5.93 g (89%) of p-[trans-4-(3-pentenyl)cyclohexyl]benzonitrile as white crystals.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04565425
出典データセットuspto-grants-1986_01
ORD IDord-9b5f81e0c1204ad4b91b9eda405ea4ac
出典メモuspto-grants-1986_01