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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1586290생성일: 2026년 10월 27일

Ammonium Chloride → 2-[2-(3,4-Dimethoxyphenyl)-4,5-dimethoxyphenyl]-4,4-dimethyl-2-oxazoline

https://huagongshe.com/reaction/1586290

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물Benzene, 4-bromo-1,2-dimethoxy-HCID 76114—
반응물MagnesiumHCID 5462224—
반응물2-(2,4,5-Trimethoxyphenyl)-4,4-dimethyl-2-oxazolineHCID 11097455—
용매TetrahydrofuranHCID 8028—
생성물2-[2-(3,4-Dimethoxyphenyl)-4,5-dimethoxyphenyl]-4,4-dimethyl-2-oxazolineHCID 2121816892.8%

반응 단계

In tetrahydrofuran (100 ml), magnesium (1.3 g) was reacted with 4-bromoveratrole (13 g) to prepare a Grignard reagent. While cooling in an ice-water bath, a solution of 2-(2,4,5-trimethoxyphenyl)-4,4-dimethyl-2-oxazoline (7.7 g) in tetrahydrofuran (100 ml) was added thereto. After stirring at room temperature for 48 hours, an aqueous saturated ammonium chloride solution (150 ml) was added and stirred for 15 minutes. Then, the mixed solution was separated to extract the aqueous layer with tetrahydrofuran (150 ml). The organic layers were combined each other and concentrated by an evaporator. The residue was dissolved in 10% hydrochloric acid (100 ml), which was washed with diethyl ether. The aqueous layer was cooled in an ice-water bath, then neutralized by adding a 20% aqueous sodium hydroxide solution. It was extracted with ethyl acetate, washed with a saturated saline solution and then dried over sodium sulfate. The solvent was distilled off to give 10 g of 2-[2-(3,4-dimethoxyphenyl)-4,5-dimethoxyphenyl]-4,4-dimethyl-2-oxazoline as a pale brown oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05942641
출처 데이터셋uspto-grants-1999_08
ORD IDord-e56a5f572a494381af91b09235b78a70
출처 메모uspto-grants-1999_08