돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 459147생성일: 2026년 10월 24일

Triethylamine → 3-(4-Hydroxy-3-methoxy-phenyl)-2-methoxy-propionic acid methyl ester

https://huagongshe.com/ko/reaction/459147

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Trifluoroacetic anhydrideHCID 9845—
반응물3-(4-Benzyloxy-3-methoxy-phenyl)-3-hydroxy-2-methoxy-propionic acid methyl esterHCID 58822925—
용매DichloromethaneHCID 6344—
생성물3-(4-Hydroxy-3-methoxy-phenyl)-2-methoxy-propionic acid methyl esterHCID 5882300886%

반응 단계

Trifluoroacetic anhydride (0.62 mL, 4.36 mmol) and triethylamine (0.62 mL, 4.36 mmol) were added to a solution of 3-(4-benzyloxy-3-methoxy-phenyl)-3-hydroxy-2-methoxy-propionic acid methyl ester (1.01 g, 2.91 mmol) in methylene chloride (30 mL) at 0° C. The resulting mixture was stirred for 4 hours at room temperature and was concentrated under vacuum. The residue was dissolved in ethyl acetate (30 mL), and 10% palladium on carbon (0.3 g) was added to the solution. The mixture was stirred under hydrogen pressure (4 atm) for 16 hours. The mixture was filtered through Celite and concentrated under vacuum. The residue was purified by silica gel column chromatography (silica gel, hexanes/ethyl acetate 7:3) to produce 3-(4-hydroxy-3-methoxy-phenyl)-2-methoxy-propionic acid methyl ester as an oil (598 mg, 86%). 1H-NMR (200.15 MHz, CDCl3): δ 6.80 (d, 1H, J=7.8), 6.7 (s, 1H), 6.62 (d, 1H, J=7.8), 3.96 (dd, 1H, J=7.8, 4.0), 3.80 (s, 3H), 3.68 (s, 3H), 3.30 (s, 3H), 3.09 (dd, 1H, J=14.2, 4.0), 2.91 (dd, 1H, J=14.2, 7.8).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07192982B2
출처 데이터셋uspto-grants-2007_03
ORD IDord-78a76c8d5c954372aba6aed127820609
출처 메모uspto-grants-2007_03