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HRID 442076作成日:2026年10月25日

Acetic Acid → 5-(3',5'-Di-tert-butyl-4'-hydroxyphenylethyl)-5-methyl-1-n-octadecylhydantoin

https://huagongshe.com/reaction/442076

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物Potassium CyanideHCID 9032—
反応物OctadecylamineHCID 15793—
反応物2-Butanone, 4-[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]-HCID 3960962—
反応物Potassium cyanateHCID 11378442—
溶媒Hydrochloric AcidHCID 313—
溶媒WaterHCID 962—
生成物5-(3',5'-Di-tert-butyl-4'-hydroxyphenylethyl)-5-methyl-1-n-octadecylhydantoinHCID 21416277—

反応手順

7.8 g (0.12 mole) of potassium cyanide in 40 ml of water is slowly added to a stirred solution of 27.6 g (0.1 mole) of 3,5-di-tert-butyl-4-hydroxyphenylethyl methyl ketone and 27.0 g (0.1 mol) of n-octadecylamine in 200 ml of glacial acetic acid at 15°-25° C. The mixture is stirred at 20°-25° C for 3.5 hours after addition is complete and then allowed to stand overnight at room temperature. The reaction mixture is then diluted with water and extracted with ether. The ether extract is dried and evaporated to dryness. The crude aminonitrile thus obtained is dissolved in 200 ml of glacial acetic acid containing 10 ml of concentrated hydrochloric acid and reacted with 16.2 g (0.2 mole) of potassium cyanate in 50 ml of water. The reaction mixture is warmed at 35°-50° C for 3 hours, then cooled and poured into water. The solid obtained is removed by filtration and then refluxed with 300 ml of 20% aqueous hydrochloric acid for 30 minutes. The solution is cooled and then desired product, 5-(3',5'-di-tert-butyl-4'-hydroxyphenylethyl)-5-methyl-1-n-octadecylhydantoin, is isolated by filtration, washed, dried and recrystallized.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04044019
出典データセットuspto-grants-1977_08
ORD IDord-a91a0e2582894908ab6e5f4923d36379
出典メモuspto-grants-1977_08