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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1800567Generated: October 29, 2026

Dimethylformamide → HCID 57387082, compound

https://huagongshe.com/reaction/1800567

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium BicarbonateHCID 516892—
Reactant3-Amino-4-fluorophenolHCID 13519180—
Reactant2-Chloro-3-(1-cyanocyclopropyl)benzoic acidHCID 66810306—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventOxalyl chlorideHCID 65578—
ProductHCID 57387082HCID 5738708298.3%

Reaction Steps

To a solution of 2-chloro-3-(1-cyanocyclopropyl)benzoic acid (4.42 g, 20 mmol) produced in Example C62(ii) in oxalyl chloride (10 mL) was added N,N-dimethylformamide (100 μL), and the mixture was stirred at room temperature for 1 hr, and concentrated to dryness under reduced pressure. This was dissolved in tetrahydrofuran (10 mL), and the solution was added dropwise with vigorous stirring to a two-layer mixture of a solution of 3-amino-4-fluorophenol (2.54 g, 20 mmol) in tetrahydrofuran (10 mL) and a solution (10 mL) of sodium hydrogen carbonate (2.70 g, 30 mmol) in water under ice-cooling. The reaction mixture was stirred at room temperature for 1 hr, and poured into water (200 mL), and the mixture was extracted with ethyl acetate (100 mL×2). The ethyl acetate layers were combined, and dried over anhydrous sodium sulfate. The insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (ethyl acetate/hexane=0/100→50/50) to give the title compound (6.50 g, 98%) as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08344135B2
Source datasetuspto-grants-2013_01
ORD IDord-0ffb88c88e054bc39a097c756d805dd5
Source noteuspto-grants-2013_01