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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 2-Methylbenzaldehyde | HCID 10722 | — |
| 반응물 | 2-(4-Bromophenyl)-4,4-dimethyl-4,5-dihydrooxazole | HCID 403395 | — |
| 반응물 | Magnesium | HCID 5462224 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-{4-[1-(2-Methylphenyl)-1-hydroxymethyl]phenyl}-4,4-dimethyl-2-oxazoline | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06642223B2 |
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| 출처 데이터셋 | uspto-grants-2003_11 |
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| ORD ID | ord-95e7f7bf20354914a3de5c0ed035316e |
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| 출처 메모 | uspto-grants-2003_11 |
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