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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2378402Generated: October 30, 2026

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

https://huagongshe.com/reaction/2378402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
Reactant4-Fluorophenylacetyl chlorideHCID 3744988—
Reactant2-(5-Methylfuran-2-yl)ethan-1-amineHCID 14933778—
Product4-Fluoro-N-[2-(5-methyl-2-furanyl)ethyl]benzamideHCID 2187484695%

Reaction Steps

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]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07470797B2
Source datasetuspto-grants-2008_12
ORD IDord-3884f672825543778583f36ce5f86f6a
Source noteuspto-grants-2008_12