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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 395395Generated: October 26, 2026

Dilithium Sulfide → Methyl 2-(difluoromethyl)-4-isobutyl-5-mercapto-6-(trifluoromethyl)-3-pyridinecarboxylate

https://huagongshe.com/reaction/395395

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDilithium SulfideHCID 10290727—
ReactantMethyl 5-bromo-2-(difluoromethyl)-4-(2-methylpropyl)-6-(trifluoromethyl)-3-pyridinecarboxylateHCID 15117750—
SolventHydrochloric AcidHCID 313—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-(difluoromethyl)-4-isobutyl-5-mercapto-6-(trifluoromethyl)-3-pyridinecarboxylateHCID 997471183%

Reaction Steps

To a stirred solution of 10.11 g (0.026 mol) of methyl 5-bromo-2-(difluoromethyl)-4-(2-methylpropyl)-6-(trifluoromethyl)-3-pyridinecarboxylate (example 122 of U.S. Pat. No. 5,019,153) in 75 mL dry DMF was added 1.42 g (0.031 mol) of lithium sulfide in one portion and the mixture was stirred overnight at room temperature. The reaction mixture was diluted with 150 mL of 10% HCl solution and extracted with ether (3×100 mL). The combined extracts were washed with water, dried (MgSO4) and evaporated. The residue was purified by kugelrohr distillation (oven temperature 100-110° C., 1.5 torr) to give 7.35 g (83%) of product as a yellow-green oil:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06605624B1
Source datasetuspto-grants-2003_08
ORD IDord-fc674029862348c7a91cee5d89176191
Source noteuspto-grants-2003_08