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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870530Generated: October 29, 2026

2-Methylnicotinic acid → HCID 178517527, compound

https://huagongshe.com/reaction/870530

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methylnicotinic acidHCID 643373—
ReactantLithium diisopropylamideHCID 2724682—
Reactant3-Fluoro-4-(trifluoromethoxy)benzonitrileHCID 17750670—
ReactantMethanedione--ethanol (1/1)HCID 19604758—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178517527HCID 178517527—

Reaction Conditions

Temperature0 °C

Reaction Steps

300 mg 2-methyl-nicotinic acid was suspended in 10 mL of tetrahydrofuran, and cooled to −70° C. with a bath of ethanol/dry ice. 3.3 mL lithium diisopropylamide (2.0 M in tetrahydrofuran/n-heptane/ethylbenzene) was added dropwise over 10 min and the mixture was stirred for 1.5 h at 0° C. After this time, it was cooled again to -70° C. and 0.9 g 3-fluoro-4-trifluoromethoxy-benzonitrile (4.1) was added quickly. Then the reaction mixture was stirred for 2 h at −70° C. and then warmed overnight to ambient temperature. The solvent was distilled off, diluted with ethyl acetate, 10 mL phosphate buffer and 5 mL 2N aqueous hydrochloric acid solution (pH 6-7). The formed precipitate was collected and dried. The resulting liquid phase was separated and the water phase extracted twice with ethyl acetate. The organic phase was dried over magnesium sulfate, concentrated and the residue suspended in ether and ethyl acetate. The precipitate was collected, dried and combined with the first precipitate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969568B2
Source datasetuspto-grants-2015_03
ORD IDord-fe4f5c4102824377b00db69c21f8a8d2
Source noteuspto-grants-2015_03