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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 400762생성일: 2026년 10월 25일

Water → Methyl 2'-ethyl-2-(methoxymethyl)-[1,1'-biphenyl]-4-carboxylate

https://huagongshe.com/reaction/400762

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Potassium CarbonateHCID 11430—
반응물2-Ethylphenylboronic Acid (contains varying amounts of Anhydride)HCID 4100862—
반응물Methyl 4-bromo-3-(methoxymethyl)benzoateHCID 58554220—
촉매HCID 178418397HCID 178418397—
용매TolueneHCID 1140—
생성물Methyl 2'-ethyl-2-(methoxymethyl)-[1,1'-biphenyl]-4-carboxylateHCID 5855417483%

반응 단계

To a solution of methyl 4-bromo-3-(methoxymethyl)benzoate, (Intermediate 28, step 2) (12 g, 0.0463 mol) in toluene (150 mL) and water (35 mL) under N2, was added 2-ethyl benzene boronic acid (9.02 g, 0.0601 mol) followed by potassium carbonate (19 g, 0.1389 mol) and Pd(PPh3)4 (2.67 g, 0.0023 mol). The reaction mixture was degassed with N2 for 10 min before heating. After 12 hours at 100° C., the reaction mixture was diluted with EtOAc. The organic layer was washed with sodium bicarbonate sat. solution (1×100 mL), water (2×100 mL) and finally with brine (1×100 mL). It was then dried over sodium sulphate and concentrated under reduced pressure. The residue was purified by chromatography (silica gel, 60-120 mesh, eluting with pet ether/EtOAc) to afford the title compound as a pale yellow liquid (12 g, 83%). 1H NMR (CDCl3, 400 MHz) δ 8.24-8.26 (1H, s), 7.99-8.01 (1H, d), 7.32-7.38 (2H, m), 7.22-7.27 (2H, m), 7.07-7.09 (1H, d), 4.12-4.21 (2H, d), 3.93-3.95 (3H, s), 3.28-3.30 (3H, s), 2.28-2.43 (2H, m), 1.01-1.05 (3H, t).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08741923B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-20884e10c0f841dc900921c058e5fb91
출처 메모uspto-grants-2014_06