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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1822283생성일: 2026년 10월 26일

Hydrochloric Acid → 3-[4-(3-Benzyloxy-5-methyl-phenoxy)-2-methyl-phenyl]-acrylic acid ethyl ester

https://huagongshe.com/reaction/1822283

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Potassium CarbonateHCID 11430—
반응물3-(Benzyloxy)-5-methylphenolHCID 10998379—
반응물3-(4-Fluoro-2-methyl-phenyl)-acrylic acid ethyl esterHCID 53717724—
용매Dimethyl SulfoxideHCID 679—
용매Diethyl EtherHCID 3283—
생성물3-[4-(3-Benzyloxy-5-methyl-phenoxy)-2-methyl-phenyl]-acrylic acid ethyl esterHCID 6907967758.6%

반응 조건

온도130 °C

반응 단계

A mixture of 3-benzyloxy-5-methyl-phenol (3.24 g, 15.1 mmol), 3-(4-fluoro-2-methyl-phenyl)-acrylic acid ethyl ester (3.15 g, 15.1 mmol) and 325 mesh potassium carbonate (2.51 g, 18.2 mmol) in dry DMSO (40 mL) is heated to 130° C. and stirred for 20 hours under N2. The reaction is cooled and acidified with 1 N HCl (30 mL). The mixture is then diluted with Et2O and extracted with water. The organic layer is dried (Na2SO4), and the solvent is removed in vacuo to afford crude product that is absorbed on silica gel and purified by flash chromatography using 9/1 hexanes/ethyl acetate to afford 3.56 g (58%) of the title compound. Rf=0.39 (4/1 hexanes/EtOAc). 1H NMR (400 MHz, CDCl3); MS (ES+) m/z mass calculated for C26H26O4 402, found 403 (M+1, 100%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07608639B2
출처 데이터셋uspto-grants-2009_10
ORD IDord-f68ddca77c1d4435a48459c8f2bbe4d8
출처 메모uspto-grants-2009_10