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HRID 327855作成日:2026年10月27日

Phenol → Benzene, (hexadecyloxy)-

https://huagongshe.com/reaction/327855

反応式

関与物質

役割名称HCID仕込み量
反応物PhenolHCID 996—
反応物TolueneHCID 1140—
反応物1-BromohexadecaneHCID 8213—
反応物Potassium HydroxideHCID 14797—
触媒Tetrabutylammonium BromideHCID 74236—
溶媒WaterHCID 962—
生成物Benzene, (hexadecyloxy)-HCID 443812998%

反応条件

温度92 °C

反応手順

A 1-liter three necked round bottom flask was charged with 100 grams (0.33 moles) of 1-bromohexadecane, 92.5 grams (0.99 moles) of phenol, 55.2 grams (0.99 moles) of potassium hydroxide, 10 grams of tetra-n-butylammonium bromide, 167 ml of toluene, and 167 ml of water. The flask was fitted with a mechanical stirrer, nitrogen inlet, condenser, thermometer and heating mantle. The reaction mixture was heated to reflux at about 92° C., under a nitrogen purge for 16 hours with constant agitation. After 16 hours, the mixture was cooled and transferred to a separatory funnel where the aqueous layer was removed and the upper toluene layer was washed three times with 200 ml 0.5N NAOH and three times with 200 ml deionized water. The toluene was removed under reduced pressure leaving 102.6 grams (98% yield) of n-hexadecyl phenyl ether. Analysis by gas chromatography showed that the product was 98.3% pure.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05274148
出典データセットuspto-grants-1993_12
ORD IDord-bf66e1cdae314981bd734c887691cbc3
出典メモuspto-grants-1993_12