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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1036868생성일: 2026년 10월 26일

Isobutylene → 2-(3-Bromophenyl)-4,4,8-trimethyl-1,2,3,4-tetrahydroquinoline-6-carbonitrile

https://huagongshe.com/reaction/1036868

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참여 물질

역할이름HCID투입량
반응물IsobutyleneHCID 8255—
반응물3-BromobenzaldehydeHCID 76583—
반응물Ytterbium triflateHCID 2733225—
반응물4-Amino-3-methylbenzonitrileHCID 7010316—
용매AcetonitrileHCID 6342—
용매Ethyl AcetateHCID 8857—
생성물2-(3-Bromophenyl)-4,4,8-trimethyl-1,2,3,4-tetrahydroquinoline-6-carbonitrileHCID 6728998726.2%

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온도85 °C

반응 단계

To a stirred solution of 4-amino-3-methyl-benzonitrile (10.3 g, 78.4 mmol) and 3-bromobenzaldehyde (9.2 mL, 78.4 mmol) in acetonitrile (150 mL) were added isobutene (21.0 mL, 313.5 mmol) and ytterbium(III) trifluoromethanesulfonate (Yb(OTf)3) (5.8 g, 9.5 mmol). The resulting mixture was stirred at 85° C. for 18 h in sealed tube. The mixture was diluted with ethyl acetate (300 mL) and washed with water (100 mL×2) and brine (100 mL×2) and then dried over anhydrous sodium sulfate. The solvent was removed in vacuo and the residue was purified by ISCO combi-flash chromatography (gradient elution, 10-30% ethyl acetate in petroleum ether) to afford 2-(3-bromo-phenyl)-4,4,8-trimethyl-1,2,3,4-tetrahydro-quinoline-6-carbonitrile (7.3 g, 26.1%) as a light yellow oil: LC/MS m/e obsd. (ESI+) [(M+H)+] 355.0 & 357.0.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08546427B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-1d2e55a5f4514e8b9eb0a1c1afb69f7f
출처 메모uspto-grants-2013_10