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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 483283생성일: 2026년 10월 26일

Iodine → 2-(4,4-Dimethyl-2-oxazolin-2-yl)-4'-n-butylbiphenyl

https://huagongshe.com/reaction/483283

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물1,1-DibromoethaneHCID 11201—
반응물4,4-Dimethyl-2-(2-methoxyphenyl)oxazolineHCID 333189—
반응물1-Butyl-4-iodobenzeneHCID 2724607—
반응물MagnesiumHCID 5462224—
반응물(4-Iodobutyl)benzeneHCID 12709818—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물2-(4,4-Dimethyl-2-oxazolin-2-yl)-4'-n-butylbiphenylHCID 1362927925%

반응 단계

A mechanically stirred solution of magnesium turnings (Mallinckrodt, for Grignard's reaction, 3.75 g., 0.154 mole) and 2-(2-methoxyphenyl)-4,4-dimethyl-2-oxazoline (30 g, 0.146 mole) in 50 mL dry tetrahydrofuran under nitrogen was prepared. To this was added a crystal of iodine, 1 mL of dibromoethane and 2 mL of neat p-Iodo n-butylbenzene to initiate the Grignard reaction. After warming to initiate the reaction, the remainder of the p-iodo-n-butylbenzene (40 g, 0.154 mole) in 50 mL dry tetrahydrofuran was added dropwise at a rate sufficient to maintain the reaction at gentle reflux. The addition took 1 hr and the reaction mixture was then heated at reflux for 3 hr. The reaction was then cooled to room temperature and 15 mL water was added dropwise to coagulate the salts. The tetrahydrofuran was decanted and the remaining solids were slurried twice with 200 mL ethyl ether and twice with 300 mL dichloromethane. Each organic extract was decanted from the solids in turn and combined and evaporated under reduced pressure to an oil. The oil was redissolved in 300 mL dichloromethane, washed once with 100 ml saturated sodium chloride solution, dried and concentrated under reduced pressure. The resulting residue was distilled under reduced pressure (0.027 Torr, 130°) to yield 2-(4,4-dimethyl-2-oxazolin-2-yl)-4'-n-butylbiphenyl as an oil, yield 25%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04578522
출처 데이터셋uspto-grants-1986_03
ORD IDord-72ecc216163440898323f1a262f06853
출처 메모uspto-grants-1986_03