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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1764135생성일: 2026년 10월 27일

Phenol, p-(1-cyclohexen-1-yl)- → alpha-[p-(1-Cyclohexyl)-phenoxy]-nonanoic acid ethyl ester

https://huagongshe.com/reaction/1764135

반응식

참여 물질

역할이름HCID투입량
반응물Phenol, p-(1-cyclohexen-1-yl)-HCID 69727—
반응물Ethyl 2-bromononan-1-oateHCID 110997—
반응물SodiumHCID 5360545—
용매EthanolHCID 702—
생성물alpha-[p-(1-Cyclohexyl)-phenoxy]-nonanoic acid ethyl esterHCID 70628623—

반응 단계

To a solution of 2.4 g of sodium in 100 ml of absolute ethanol are added initially 15 g of p-(1-cyclohexenyl)-phenol in a small amount of absolute ethanol at room temperature under anhydrous conditions and with stirring. 34 Grams of α-bromo-nonanoic acid ethyl ester are then added dropwise and the reaction mixture is stirred for 24 hours at 50° C. The ethanol is subsequently stripped off in vacuo and the residue is partitioned between water and ice-cold N sodium hydroxide solution. The organic phase is washed until neutral, dried over sodium sulphate and concentrated in vacuo. The residue yields the crude α-[p-(1-cyclohexyl)-phenoxy]-nonanoic acid ethyl ester of the formula ##STR15## in the form of an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04115416
출처 데이터셋uspto-grants-1978_09
ORD IDord-b135ba77b3ca44ea8d9fb59e182d5601
출처 메모uspto-grants-1978_09