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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 518147생성일: 2026년 10월 26일

Methyl Acrylate → (E)-3-{1'-tert-butoxycarbonyl-4-oxo-spiro[chromane-2,4'-piperidine]-6-yl}-acrylic acid methyl ester

https://huagongshe.com/reaction/518147

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참여 물질

역할이름HCID투입량
반응물Methyl AcrylateHCID 7294—
반응물TriphenylphosphineHCID 11776—
반응물tert-Butyl 6-bromo-4-oxospiro[chroman-2,4'-piperidine]-1'-carboxylateHCID 2794759—
촉매palladium(II) acetateHCID 167845—
용매DimethylformamideHCID 6228—
생성물(E)-3-{1'-tert-butoxycarbonyl-4-oxo-spiro[chromane-2,4'-piperidine]-6-yl}-acrylic acid methyl esterHCID 5295208756.5%

반응 조건

온도100 °C

반응 단계

A mixture of 6-bromo-4-oxo-spiro[chromane-2,4′-piperidine]-1′-carboxylic acid tert-butyl ester (1.04 g, 2.62 mmol), Pd(OAc)2 (59 mg, 0.262 mmol), PPh3 (137 mg, 0.52 mmol), TEA (0.73 ml, 5.2 mmol), methyl acrylate (0.47 ml, 5.2 mmol) in dry DMF (10 ml) was heated at 100° C. for 8 h. The mixture was cooled down to RT, filtered on a celite pad and washed with AcOEt (100 ml). The filtrate was washed with NH4Cl and saturated NaHCO3 solution and brine. The organic phase was dried over Na2SO4 and evaporated under vacuum. The crude residue was purified by column chromatography (eluent: hexane/AcOEt 90:10 to 70:30) to give (E)-3-{1′-tert-butoxycarbonyl-4-oxo-spiro[chromane-2,4′-piperidine]-6-yl}-acrylic acid methyl ester (594 mg) as a light yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09115148B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-f9ad2718e899439abea27c2aeec88001
출처 메모uspto-grants-2015_08