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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2387154Generated: October 27, 2026

3-Fluorobenzonitrile → Methyl 3-fluorobenzenecarboximidoate

https://huagongshe.com/reaction/2387154

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, 410n 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 numberUS08268835B2
Source datasetuspto-grants-2012_09
ORD IDord-cd1b83ab1f3c40ff9f13d2fd147a4e6d
Source noteuspto-grants-2012_09