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HRID 1077395作成日:2026年10月26日

4-Butoxyphenol → 4-(6-Methacryloyloxyhexyloxy)-benzoic acid-4-n-butoxyphenyl ester

https://huagongshe.com/reaction/1077395

反応式

関与物質

役割名称HCID仕込み量
反応物4-ButoxyphenolHCID 31233—
反応物4-{[6-(Methacryloyloxy)hexyl]oxy}benzenecarboxylic acidHCID 3730344—
溶媒TetrahydrofuranHCID 8028—
溶媒TriethylamineHCID 8471—
生成物4-(6-Methacryloyloxyhexyloxy)-benzoic acid-4-n-butoxyphenyl esterHCID 19431246—

反応手順

6.1 g of 4-(6-methacryloyloxyhexyloxy)benzoic acid were converted to the acid chloride in a manner similar to example 6. This substance was taken up in 100 ml of tetrahydrofuran (THF) and added dropwise at 0° to 5° C. to a stirred solution of 3.3 g of hydroquinone monobutyl ether in 100 ml of THF and 4 ml of triethylamine. The mixture was stirred for a further 3 hours at room temperature and the triethylamine hydrochloride was then filtered out. The filtrate was evaporated to dryness and the residue dissolved in 50 ml of dichloromethane. The solution was washed several times with water, dried with sodium sulphate and the solvent then distilled off. The crude product so obtained was purified by column chromatography and recrystallisation from n-hexane.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05543267
出典データセットuspto-grants-1996_08
ORD IDord-976b6cb7b19143f094aa497e49fe319a
出典メモuspto-grants-1996_08