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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2100050생성일: 2026년 10월 27일

Triethylamine → 1,1-Dimethylethyl(2E)-3-{4-[(4-hydroxyphenyl)(tetrahydro-4H-thiopyran-4-ylidene)methyl]phenyl}-2-propenoate

https://huagongshe.com/reaction/2100050

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물tert-Butyl acrylateHCID 15458—
반응물Tri-o-tolylphosphineHCID 80271—
반응물4-[(4-Bromophenyl)(tetrahydro-4H-thiopyran-4-ylidene)methyl]phenolHCID 68654429—
촉매palladium(II) acetateHCID 167845—
용매AcetonitrileHCID 6342—
생성물1,1-Dimethylethyl(2E)-3-{4-[(4-hydroxyphenyl)(tetrahydro-4H-thiopyran-4-ylidene)methyl]phenyl}-2-propenoateHCID 68978299—

반응 조건

온도85 °C

반응 단계

Reagents 36 (0.32 g, 0.886 mmol), t-butyl acrylate (0.78 mL, 5.31 mmol), Pd(OAc)2 (0.042 g, 0.186 mmol), P(o-tolyl)3 (0.12 g, 0.381 mmol) and Et3N (0.74 mL, 5.31 mmol) were added to a flask containing CH3CN (13 mL) and the reaction mixture was heated at 85° C. for 24 h. The reaction mixture was allowed to cool at RT and partitioned between water and EtOAc. The organic layer was separated, washed with brine, dried (MgSO4), filtered, and the filtrate was concentrated to give the crude product. The crude product was purified by flash column chromatography on silica gel using a hexanes:EtOAc gradient (100:0 to 50:50) to give compound 37 as a yellow foam. 1H NMR (400 MHz, DMSO-d6): δ 1.46 (s, 9H), 2.65-2.66 (m, 5H), 6.45 (d, J=16 Hz, 1H), 6.68 (d, J=8.4 Hz, 2H), 6.87 (d, J=8.5 Hz, 2H), 7.09 (d, J=8.1 Hz, 2H), 7.49 (d, J=16.1 Hz, 1H), 7.60 (d, J=8.1 Hz, 2H), 9.37 (s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07569601B2
출처 데이터셋uspto-grants-2009_08
ORD IDord-a7783ce1f834456bb17e8f98adf70b67
출처 메모uspto-grants-2009_08