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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 614067생성일: 2026년 10월 26일

3-Chloro-2-methyl-1-propene → alpha-Methallyl-alpha,3,3-trimethyl-5-norbornene-2-methanol

https://huagongshe.com/reaction/614067

반응식

참여 물질

역할이름HCID투입량
반응물3-Chloro-2-methyl-1-propeneHCID 11241—
반응물Ammonium ChlorideHCID 25517—
반응물1-(3,3-Dimethylbicyclo(2.2.1)hept-5-en-2-yl)ethan-1-oneHCID 162511—
반응물MagnesiumHCID 5462224—
용매Diethyl EtherHCID 3283—
생성물alpha-Methallyl-alpha,3,3-trimethyl-5-norbornene-2-methanolHCID 21319801106.5%

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 one-half 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 one-half 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04143074
출처 데이터셋uspto-grants-1979_03
ORD IDord-a38d6262732c4b6ba9d404ebe2a9dda5
출처 메모uspto-grants-1979_03