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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 478340생성일: 2026년 10월 25일

2-Methylbenzaldehyde → 2-{4-[1-(2-Methylphenyl)-1-hydroxymethyl]phenyl}-4,4-dimethyl-2-oxazoline

https://huagongshe.com/reaction/478340

반응식

참여 물질

역할이름HCID투입량
반응물2-MethylbenzaldehydeHCID 10722—
반응물2-(4-Bromophenyl)-4,4-dimethyl-4,5-dihydrooxazoleHCID 403395—
반응물MagnesiumHCID 5462224—
용매TetrahydrofuranHCID 8028—
생성물2-{4-[1-(2-Methylphenyl)-1-hydroxymethyl]phenyl}-4,4-dimethyl-2-oxazolineHCID 18001016—

반응 단계

To a solution of 2-(4-bromophenyl)-4,4-dimethyl-2-oxazoline (1 g) in dry tetrahydrofuran (10 ml) are added dropwise magnesium (526 mg) and dry tetrahydrofuran (50 ml) under refluxing. The heating of the mixture is stopped, and thereto is added 2-(4-bromphenyl)-4,4-dimethyl-2-oxazoline (4 g) at a slowly refluxing rate, during which the mixture is stirred for 30 minutes, and then thereto is added o-tolualdehyde (2.16 ml) under ice-cooling. The mixture is stirred under ice-cooling for one hour, and stirred at room temperature for two hours, and the reaction is quenched with adding thereto a saturated aqueous ammonium chloride solution. The mixture is extracted with ethyl acetate, and the organic layer is washed successively with 1N hydrochloric acid, a saturated aqueous sodium hydrogen carbonate solution and a saturated sodium chloride solution, dried over magnesium sulfate, and concentrated. The residue is purified by silica gel column chromatography (solvent; n-hexane:ethyl acetate=4˜2:1) to give 2-{4-[1-(2-methylphenyl)-1-hydroxymethyl]phenyl}-4,4-dimethyl-2-oxazoline (3.07 g) as white powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06642223B2
출처 데이터셋uspto-grants-2003_11
ORD IDord-95e7f7bf20354914a3de5c0ed035316e
출처 메모uspto-grants-2003_11