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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 264838Generated: November 2, 2026

Methylamine → 2,2-bis(fluoromethyl)-N-methyl-6-nitro-2H-1-benzopyran-4-carboxamide

https://huagongshe.com/reaction/264838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantPotassium CarbonateHCID 11430—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant2,2-bisfluoromethyl-6-nitro-2H-1-benzopyran-4-carboxylic acidHCID 21194987—
SolventTetrahydrofuranHCID 8028—
Product2,2-bis(fluoromethyl)-N-methyl-6-nitro-2H-1-benzopyran-4-carboxamideHCID 1903704115.9%

Reaction Steps

To a mixture of 0.78 g of 2,2-bis(fluoromethyl)-6-nitro-2H-1-benzopyran-4-carboxylic acid and 5 ml of tetrahydrofuran was added 0.67 g of 1,1'-carbonyldiimidazole with stirring under ice-cooling and the mixture was stirred for 1 hour. Then, 6.3 ml of 40% methylamine (methanol solution) was added therein. The resultant mixture was stirred under ice-cooling for 1 hour and then at room temperature for 14 hours. An aqueous potassium carbonate solution was added therein and the mixture was extracted with ether. An organic layer was washed with water and dried, and the solvent was distilled. The obtained residue was purified according to silica gel column chromatography (developing solution, MeOH:CH2Cl2 =1:99) to obtain 0.13 g of 2,2-bis(fluoromethyl)-N-methyl-6-nitro-2H-1-benzopyran-4-carboxamide with a melting point of 178°-179° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05646308
Source datasetuspto-grants-1997_07
ORD IDord-c5d156e79f4c4534b588cc877d04b46f
Source noteuspto-grants-1997_07