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HRID 1733532作成日:2026年10月27日

1,2-Dimethoxyethane → 2-[4-(Hexadecylamino)phenyl]oxazoline

https://huagongshe.com/reaction/1733532

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-DimethoxyethaneHCID 8071—
反応物2-Bromoethylamine hydrobromideHCID 2774217—
反応物4-Hexadecylaminobenzoyl chloride hydrochlorideHCID 13255322—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒TriethylamineHCID 8471—
生成物2-[4-(Hexadecylamino)phenyl]oxazolineHCID 20437370—

反応手順

To a slurry of 15 g. of 2-bromoethylamine hydrobromide in 150 ml. of glyme was added simultaneously solutions of 31 g. of 4-(hexadecylamino)benzoyl chloride hydrochloride in 60 ml. of glyme and 50 cc. of triethylamine (dropwise). Upon addition of 0.5 g. of 4-dimethylaminopyridine the "solution" was stirred at room temperature overnight. The solution was refluxed for one hour and filtered. The solid was oven dried and portitioned between CH2Cl and water. The layers were separated and the organic phase dried over MgSO4. The organic layer was concentrated to about 100 ml. and 4-(hexadecylamino)benzoyl chloride hydrochloride diluted with an equal volume of hexane. The combined product (4.15 g.) was preabsorbed on 40 g. of silica III and placed on a column of silica III (800 g.). Fractions were collected by U.V. (CH2Cl2 -EtOH 97-3) and samples with the same TLC combined giving 3.8 g. after recrystallization from cyclohexane. A 210 mg. sample was recrystallized from acetonitrile and CH2Cl2 /hexane giving 149 mg., m.p. 123°-125° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04242273
出典データセットuspto-grants-1980_12
ORD IDord-684f59d8ebb8458c8c5295644234e376
出典メモuspto-grants-1980_12