Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 26187생성일: 2026년 10월 26일
3-Chloro-2-methyl-1-propene → alpha-Methallyl-alpha,3,3-trimethyl-5-norbornene-2-methanol
https://huagongshe.com/reaction/26187
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 3-Chloro-2-methyl-1-propene | HCID 11241 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | 1-(3,3-Dimethylbicyclo(2.2.1)hept-5-en-2-yl)ethan-1-one | HCID 162511 | — |
| 반응물 | Magnesium | HCID 5462224 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | alpha-Methallyl-alpha,3,3-trimethyl-5-norbornene-2-methanol | HCID 21319801 | 106.5% |
반응 단계
Into a 1 liter reaction flask equipped with a reflux condenser, thermometer, stirrer, dropping funnel and nitrogen inlet tube are placed 12 g (0.5 moles) of magnesium turnings and 250 cc anhydrous diethyl ether. Over a 2 hour period, 45.3 g (0.5 moles) of methallyl chloride is added. The Grignard solution is stirred for 1/2 hour and 28 g of 2-acetyl-3,3-dimethyl-5-norbornene is added over a 20 minute period. The mixture is stirred at reflux for 1/2 hour and then is hydrolyzed by the addition of saturated ammonium chloride solution. The organic layer is washed with water and dried over magnesium sulfate. The mixture is then filtered and the solvent evaporated to yield 40 g of an oil, which is then fractionated on a micro Vigreux column after adding thereto 5 g Primol® and a trace quantity of Ionox®.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04148826 |
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| 출처 데이터셋 | uspto-grants-1979_04 |
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| ORD ID | ord-8d98939ba4254bfdae96417e380f1482 |
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| 출처 메모 | uspto-grants-1979_04 |
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