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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355685Generated: October 29, 2026

2-Fluorobenzoyl chloride → HCID 54292599, compound

https://huagongshe.com/reaction/355685

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluorobenzoyl chlorideHCID 9808—
Reactant2-Amino-3-NitrophenolHCID 4115495—
SolventPyridineHCID 1049—
ProductHCID 54292599HCID 5429259985.1%

Reaction Steps

1.57 g (10 mmol) of 2-amino-3-nitrophenol was dissolved in 20 ml of pyridine and 3.36 g (21 mmol) of 2-fluorobenzoyl chloride was added thereto under stirring. After heating under reflux for 4 hours, the mixture was concentrated. Then dilute hydrochloric acid and ethyl acetate were added thereto. The organic layer was separated and washed with water. After concentrating, 20 ml of tetrahydrofuran and 20 ml of 1N sodium hydroxide were added and the mixture was heated under reflux for 4 hours. After cooling, it was neutralized with hydrochloric acid and concentrated. After adding ethyl acetate and water, the organic layer was separated, washed with water and dried over magnesium sulfate. After concentrating, the residue was purified by silica gel column chromatography. Thus 2.35 g of 2-fluoro-N-(2-hydroxy-6-nitrophenyl)benzamide was obtained. 553 mg (2 mmol) of this powder was dissolved in 20 ml of dimethylformamide and 332 mg (2.4 mmol) of potassium carbonate and 20 mg of a copper powder were added thereto. After heating under reflux for 3 hours and concentrating, ethyl acetate and dilute hydrochloric acid were added to the residue. The formed insoluble matters were filtered off and the organic layer was separated, washed with water, dried over magnesium sulfate and concentrated. Then the residue was purified by silica gel column chromatography. Thus 400 mg of the title compound was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05834462
Source datasetuspto-grants-1998_11
ORD IDord-e7ab4743f61f40c4aab7d4ff2e6f6c1a
Source noteuspto-grants-1998_11