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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1716006생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1716006

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 번호US07799828B2
출처 데이터셋uspto-grants-2010_09
ORD IDord-a74748fea9844043b63699dfe988baab
출처 메모uspto-grants-2010_09