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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 645333생성일: 2026년 10월 25일

Hydrochloric Acid → 2,3,8a-trimethyl-3,4,4a,5,8,8a-hexahydro-1(2H)-naphthalenone

https://huagongshe.com/reaction/645333

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물1,3-ButadieneHCID 7845—
반응물Ethylaluminum dichlorideHCID 11237—
반응물2-Cyclohexen-1-one, 2,5,6-trimethyl-HCID 89264—
용매DichloromethaneHCID 6344—
생성물2,3,8a-trimethyl-3,4,4a,5,8,8a-hexahydro-1(2H)-naphthalenoneHCID 57429441—

반응 단계

In a 1 liter round-bottomed flask, at room temperature, were successively added CH2Cl2 (400 ml), BHT (100 mg) and a 1 M solution of EtAlCl2 in hexanes (80 ml; 0.08 mol). 2,5,6-trimethylcyclohex-2-en-1-one (55.2 g, 0.4 mol, 3:2 mixture of two isomers) was added dropwise, while maintaining the internal temperature below 30° C. Then butadiene (43.2 g, 0.8 mol) was added in one portion. The reaction was stirred at room temperature for 15 days. The reaction was then poured onto cold 5% aqueous HCl and extracted twice with ether. The organic layers were washed with saturated aqueous NaHCO3, water and brine and dried over solid sodium sulfate. The crude product was distilled to give 50 g of a liquid which was then chromatographed on silicagel (heptane:ethyl acetate 49:1) then purified by bulb-to-bulb distillation (B.P.=90° C./0.021 mbar) to give the totle compound (39.43 g, 0.205 mol, 51%) as a 3:2 mixture of diastereoisomers.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07704933B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-579305bd9e9742e297fe5c0214d13473
출처 메모uspto-grants-2010_04