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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1017865생성일: 2026년 10월 26일

Hydrogen Bromide → 1'-Benzyl-3-(4-isopropylphenyl)-4,6,7-trimethylspiro[benzofuran-2(3H), 4'-piperidine]

https://huagongshe.com/reaction/1017865

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen BromideHCID 260—
반응물Sodium HydroxideHCID 14798—
반응물(1-Benzyl-4-piperidyl)(4-isopropylphenyl)(3,4,6-trimethyl-2-methoxyphenyl)methanolHCID 21961358—
용매Acetic AcidHCID 176—
생성물1'-Benzyl-3-(4-isopropylphenyl)-4,6,7-trimethylspiro[benzofuran-2(3H), 4'-piperidine]HCID 2196134384.9%

반응 단계

To a solution of (1-benzyl-4-piperidyl)(4-isopropylphenyl) (3,4,6-trimethyl-2-methoxyphenyl)methanol (5.61 g, 11.89 mmol) in acetic acid (40 ml) was added a 47% hydrobromic acid (50 ml) and the resulting mixture was refluxed with heating for 13 hours. The reaction mixture was cooled down to room temperature and then an 8 N aqueous solution of sodium hydroxide was added into the mixture until it became basic. The product was extracted with ethyl acetate. T he extracts were washed with an aqueous saturated solution of sodium chloride, dried on magnesium sulfate, filtered, and then concentrated under reduced pressure. The residue was crystallized from hexane to obtain 4.44 g (76% yield) of the title compound. Melting point: 125-128° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06479536B1
출처 데이터셋uspto-grants-2002_11
ORD IDord-8185959be2dc4190b6b19aef3e7fed63
출처 메모uspto-grants-2002_11