돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1733532생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1733532

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DimethoxyethaneHCID 8071—
반응물2-Bromoethylamine hydrobromideHCID 2774217—
반응물4-Hexadecylaminobenzoyl chloride hydrochlorideHCID 13255322—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매TriethylamineHCID 8471—
생성물2-[4-(Hexadecylamino)phenyl]oxazolineHCID 20437370—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04242273
출처 데이터셋uspto-grants-1980_12
ORD IDord-684f59d8ebb8458c8c5295644234e376
출처 메모uspto-grants-1980_12