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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 272357생성일: 2026년 10월 26일

Formaldehyde → 3-(4-Isopropylphenyl)-1',4,6,7-tetramethylspiro[benzofuran-2(3H),4'-piperidine]

https://huagongshe.com/reaction/272357

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참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물3-(4-Isopropylphenyl)-4,6,7-trimethylspiro[benzofuran-2(3h),4'-piperidine]hydrochlorideHCID 21961353—
용매AcetonitrileHCID 6342—
생성물3-(4-Isopropylphenyl)-1',4,6,7-tetramethylspiro[benzofuran-2(3H),4'-piperidine]HCID 2196131240%

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온도0 °C

반응 단계

To a suspension of 3-(4-isopropylphenyl)-4,6,7-trimethylspiro[benzofuran-2(3H),4′-piperidine]hydrochloride (389.6 mg, 1.01 mmol) in acetonitrile (5 ml) was added 37% formalin (2.0 ml) and the mixture was cooled to 0° C. Sodium cyanoborohydride (101.8 mg, 1.62 mmol) was added into this mixture and the mixture was stirred at room temperature for 1 hour. The reaction mixture was concentrated under reduced pressure and an aqueous saturated solution of sodium hydrogen carbonate was added to the residue. The product was extracted twice with ethyl acetate. The combined extracts were washed with water, dried on magnesium sulfate, filtered, and then concentrated under reduced pressure. The residue was subjected to column chromatography (on Chromatorex NHDM1020 (trade name, manufactured by Fuji Silysia Chemical Ltd.); hexane-ethyl acetate 10:1) to obtain 145.0 mg (40% yield) of the title compound. Melting point: 63-64° C. (Petroleum ether)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07456162B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-d5a6597f1caa44b49f453a2c6b0e67a8
출처 메모uspto-grants-2008_11