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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1805928생성일: 2026년 10월 23일

Sodium Hydroxide → 4-(2-Hydroxyethyl)-2-methoxyphenyl acetate

https://huagongshe.com/ko/reaction/1805928

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물Homovanillyl alcoholHCID 16928—
반응물1-Acetyl-1H-1,2,3-triazolo[4,5-b]pyridineHCID 702889—
용매Hydrochloric AcidHCID 313—
용매TetrahydrofuranHCID 8028—
생성물4-(2-Hydroxyethyl)-2-methoxyphenyl acetateHCID 67376667—

반응 조건

온도25 °C

반응 단계

A solution of 1-acetyl-1H-1,2,3-triazolo[4,5-b]pyridine (0.964 g, 5.95 mmol) in dry THF (24 mL) was added to a solution of homovanillyl alcohol (1.00 g, 5.95 mmol) in 1N aq. NaOH (5.95 mL, 5.95 mmol) at 25° C. The reaction was stirred at 25° C. for 60 min. The reaction was diluted with 1N HCl (40 mL) and extracted with Et2O (3×50 mL). The combined extracts were dried (MgSO4) and concentrated in vacuo to give the crude product. This was purified by flash chromatography (Biotage Horizon, 40M, Si, ˜30 mL/min, 100% hexanes for 144 mL, gradient to 50% EtOAc in hexanes over 360 mL, gradient to 100% EtOAc over 1944 mL) to afford 4-(2-hydroxyethyl)-2-methoxyphenyl acetate, as a colorless oil. Rf=0.71 (EtOAc). LCMS calc.=233.1; found=233.1 (M+Na)+. 1H NMR (500 MHz, CDCl3): δ 6.95 (d, J=8.0 Hz, 1 H); 6.83 (d, J=1.8 Hz, 1 H); 6.79 (dd, J=1.8, 8.0 Hz, 1 H); 3.88 (t, J=6.6 Hz, 2 H), 3.84 (s, 3 H); 2.82 (t, J=6.5 Hz, 2 H); 2.30 (s, 3 H); 1.76 (s, 1 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08354454B2
출처 데이터셋uspto-grants-2013_01
ORD IDord-c4035f4e93494d4e998e5477266b7216
출처 메모uspto-grants-2013_01