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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1441797생성일: 2026년 10월 26일

Tetrahydrofuran → 4-Fluoro-N-[2-(5-methyl-2-furanyl)ethyl]benzamide

https://huagongshe.com/reaction/1441797

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물TriethylamineHCID 8471—
반응물4-Fluorophenylacetyl chlorideHCID 3744988—
반응물2-(5-Methylfuran-2-yl)ethan-1-amineHCID 14933778—
생성물4-Fluoro-N-[2-(5-methyl-2-furanyl)ethyl]benzamideHCID 2187484695%

반응 단계

4-Fluorophenylacetyl chloride (0.290 mL, 2.44 mmol) was added dropwise to a solution of β-(5-methyl-2-furanyl)ethanamine (300 mg, 2.44 mmol, made according to the procedure of Yur'ev et al. J. Gen. Chem. USSR (Engl. Transl.) 33, 3444-8 (1963)) in THF (2.5 mL) at rt, followed by the dropwise addition of Et3N (0.340 mL, 2.44 mmol). Once the starting material was consumed, as was evident by HPLC, the reaction was quenched with H2O and extracted with CH2Cl2. The combined organic layers were dried over MgSO4 and concentrated under reduced pressure. Purification by flash chromatography on silica gel eluting with a gradient of 0-50% EtOAc/hexane gave 523 mg (95%) of compound 237A as a white solid. HPLC: 99% at 2.84 min (retention time) (Phenomenex-prime S5-C18 column 4.6×50 mm eluting with 10-90% aqueous methanol over 4 minutes containing 0.2% phosphoric acid, 4 mL/min, monitoring at 220 nm). MS (ES): m/z 248.15 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07655689B2
출처 데이터셋uspto-grants-2010_02
ORD IDord-0a07f5257e424f85bdeaaf3a28935b54
출처 메모uspto-grants-2010_02