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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1921279Generated: October 31, 2026

2,6-Difluoroaniline → HCID 67056864, compound

https://huagongshe.com/reaction/1921279

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-DifluoroanilineHCID 79647—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantHCID 13794930HCID 13794930—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67056864HCID 6705686420.2%

Reaction Steps

To a solution of (2,6-difluorophenyl)amine (15.5 g) in THF (140 mL) was added dropwise an 1 M THF solution of lithium 1,1,1,3,3,3-hexamethyldisilazan-2-ide (120 mL) at 0° C. under a nitrogen atmosphere, and the mixture was stirred at the same temperature for 30 min. To the solution was added a solution of dimethyl (2E,4Z)-4-(methoxymethylene)-2-pentenedioate (20 g) in THF (60 mL) at 0° C., and the resulting mixture was stirred at the same temperature for 2 hr. The reaction was quenched with a mixture of EtOAc (200 mL) and 0.5 M HCl (200 mL). The aqueous layer was extracted with EtOAc (200 mL). The organic layers were combined, washed with brine, dried over MgSO4, filtered and evaporated in vacuo. The residue was diluted with MeOH (100 mL), and to the resulting solution was added 28% sodium methoxide in MeOH (38.6 mL). The resulted mixture was heated to reflux for 6 hr under a nitrogen atmosphere. The reaction mixture was concentrated under reduced pressure and the residue was partitioned between EtOAc (200 mL) and 1 M HCl (300 mL). The aqueous layer was separated and extracted with EtOAc (200 mL). The organic layers were combined, washed with saturated aqueous NaHCO3 (300 mL) and brine successively, dried over MgSO4 and evaporated in vacuo. The residue was triturated with IPE, and the precipitates produced were collected by filtration to give methyl 1-(2,6-difluorophenyl)-6-oxo-1,6-dihydro-3-pyridinecarboxylate (5.34 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173684B2
Source datasetuspto-grants-2012_05
ORD IDord-01a1edaf031e4e0ea94ad1e0ca07687b
Source noteuspto-grants-2012_05