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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2186546생성일: 2026년 10월 26일

1-(5,5,8,8-Tetramethyl-5,6,7,8-tetrahydro-naphthalen-2-yl)-1-hexanone → 2-Hexyl-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalene

https://huagongshe.com/reaction/2186546

반응식

참여 물질

역할이름HCID투입량
반응물1-(5,5,8,8-Tetramethyl-5,6,7,8-tetrahydro-naphthalen-2-yl)-1-hexanoneHCID 22456876—
촉매Hydrochloric AcidHCID 313—
촉매PalladiumHCID 23938—
용매EthanolHCID 702—
생성물2-Hexyl-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthaleneHCID 2300253092.2%

반응 단계

A solution of 13.8 g of 1-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-naphthalen-2-yl)-1-hexanone (from Example 1.1) in 200 ml ethanol abs., containing 2 g of palladium on carbon 10% and 3 drops of HCl 25%, was subjected to H2 atmosphere for 3 hours (until consumption of theoretical amount H2 is reached and thin layer chromatography showed no more starting material was present). The mixture was filtered and concentrated in vacuo. The residue was diluted in 200 ml ether, dried over MgSO4, filtered and concentrated in vacuo, giving a yellow oil. The crude product was distilled under vacuum (T=120° C. at 0.08 bar), yielding a pale yellow oil (12.1 g). B.p. 120° C. at 0.08 bar.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06403810B2
출처 데이터셋uspto-grants-2002_06
ORD IDord-d77808b5a6794a1c88c7062489e0f284
출처 메모uspto-grants-2002_06