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HRID 1764141作成日:2026年10月27日

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

https://huagongshe.com/reaction/1764141

反応式

関与物質

役割名称HCID仕込み量
反応物Phenol, p-(1-cyclohexen-1-yl)-HCID 69727—
反応物Ethyl 2-bromodecanoateHCID 95581—
反応物SodiumHCID 5360545—
溶媒EthanolHCID 702—
生成物alpha-[p-(1-Cyclohexenyl)-phenoxy]-decanoic acid ethyl esterHCID 53893361—

反応手順

To a solution of 1.6g of sodium in 100 ml of absolute ethanol, 10 g of p-(1-cyclohexenyl)-phenol in a small amount of absolute ethanol are added at room temperature under anhydrous conditions and with stirring. 10 g of α-bromo-decanoic acid ethyl ester are then added dropwise and the reaction mixture is stirred up 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-cyclohexenyl)-phenoxy]-decanoic acid ethyl ester of the formula ##STR21## in the form of an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04115416
出典データセットuspto-grants-1978_09
ORD IDord-e8278a725ff241229debd445f2469cfd
出典メモuspto-grants-1978_09