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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606644Generated: October 30, 2026

Tetrahydrofuran → HCID 67047531, compound

https://huagongshe.com/reaction/606644

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant2,4-Difluoro-3-methoxybenzoic acidHCID 3780555—
ReactantHCID 10103284HCID 10103284—
Reactant2-Methyl-6-nitrobenzoic anhydrideHCID 10472648—
SolventWaterHCID 962—
SolventTriethylamineHCID 8471—
ProductHCID 67047531HCID 67047531—

Reaction Steps

To 376 mg of the 2,4-difluoro-3-methoxybenzoic acid was added 40 mL of tetrahydrofuran. After adding 0.75 ml of triethylamine, 20 mg of N,N-dimethylaminopyridine and 689 mg of 2-methyl-6-nitrobenzoic anhydride to this solution, the mixture was stirred at room temperature. After 2 hours, mixed acid anhydrides were confirmed by TLC, and 430 mg of ethyl N,N-dimethylaminoacrylate was added dropwise thereto. After completion of the dropwise addition, the mixture was stirred for 24 hours. After completion of the reaction, water was added to the reaction mixture, and the separated solution was extracted with ethyl acetate and dried with anhydrous sodium sulfate. After removing the sodium sulfate by filtration, the filtrate was concentration under reduced pressure to obtain 511 mg of a dark brown oily product. The resulting residue was purified by silica gel column chromatography to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915418B2
Source datasetuspto-grants-2011_03
ORD IDord-9bba04e7dd7745a8a606ba1b20ccd3cb
Source noteuspto-grants-2011_03