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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 859762Generated: October 26, 2026

3-Fluorobenzonitrile → Methyl 3-fluorobenzenecarboximidoate

https://huagongshe.com/reaction/859762

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-FluorobenzonitrileHCID 67880—
ReactantHCID 178418582HCID 178418582—
SolventMethanolHCID 887—
ProductMethyl 3-fluorobenzenecarboximidoateHCID 146855771,000.1%

Reaction Steps

MeONa (2.35 g, 41 mmol) was added to a stirred solution of 3-fluorobenzonitrile (50.0 g, 413 mmol) in methanol (300 mL). The mixture was stirred at room temperature for 3 days and concentrated in vacuo. The residue was dissolved in ether (300 mL), washed with water (2×150 mL), brine (150 mL), dried with Na2SO4, and concentrated in vacuo to afford 62.8 g (99%) of methyl 3-fluorobenzenecarboximidoate. Methylhydrazine (21.8 mL, 410 n mmol) was added to a stirred solution of methyl 3-fluorobenzenecarboximidoate (62.8 g, 410 mmol) in THF (350 mL). The mixture was stirred at room temperature for 3 days, then. Then methyl 2,2-diethoxyethanimidoate (66.1 g, 410 mmol) and acetic acid (37.5 mL, 656 mmol) were added. The mixture was stirred for 24 h. The reaction was diluted with CH2Cl2 (500 mL), and the formed precipitate was filtered off. The filtrate was washed with 10% citric acid (2×200 mL), water (300 mL), brine (200 mL), dried with Na2SO4, and concentrated in vacuo. The residue was subjected to flash chromatography on silica gel using 1% MeOH/CHCl3 as eluent to give 24.0 g (21%) of the title product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07151105B2
Source datasetuspto-grants-2006_12
ORD IDord-ba787226205c4f1babf97e9ca0864510
Source noteuspto-grants-2006_12