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HRID 9255作成日:2026年10月23日

Acetone → 2,6-Diallyl4-benzyloxyphenol

https://huagongshe.com/ja/reaction/9255

反応式

関与物質

役割名称HCID仕込み量
反応物AcetoneHCID 180—
反応物MonobenzoneHCID 7638—
反応物Allyl bromideHCID 7841—
反応物Potassium CarbonateHCID 11430—
生成物2,6-Diallyl4-benzyloxyphenolHCID 21985951—

反応手順

To a solution of starting 4-benzyloxyphenol (20 g) in acetone (800 mL) were added allylbromide (50 mL) and K2CO3 (60 g). The reaction mixture was refluxed overnight. After cooling to the room temperature, the insoluble materials were removed by filtration. The filtrate was concentrated in vac. The residue was partitioned between ethyl ether (500 mL) and 2N aqueous NaOH (200 mL). The organic layer was washed with water and brine, dried over anhydrous MgSO4, filtered, and concentrated in vac. to give the desired product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091230B2
出典データセットuspto-grants-2006_08
ORD IDord-1782f4c6e18d44388356e24fbc39135b
出典メモuspto-grants-2006_08