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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 487856Generated: October 31, 2026

Hydrochloric Acid → HCID 20098198, compound

https://huagongshe.com/reaction/487856

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHexaneHCID 8058—
Reactant3-BromothiopheneHCID 13383—
ReactantMethyl 2-(difluoromethyl)-5-formyl-4-(2-methylpropyl)6-(trifluoromethyl)-3-pyridinecarboxylateHCID 15107640—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 20098198HCID 2009819868.9%

Reaction Conditions

Temperature-70 °C

Reaction Steps

To a solution of 3-bromothiophene (4 g 24.5 mmol) in dry THF (80 mL) cooled to -70° C. was added dropwise 2.5M n-BuLi in hexane (11 mL, 27.5 mmol). The mixture was stirred for one-half h. A solution of methyl 2-(difluoromethyl)-5-formyl-4-(2-methylpropyl)-6-(trifluoromethyl)-3-pyridinecarboxylate (6.6 g, 19.5 mmol) in anhydrous THF (20 mL) was added dropwise and stirring was continued for 1 h while the temperature was maintained at -70° C. The mixture was allowed to warm to RT and then poured into iced water, acidified with conc. HCl and extracted with methylene chloride. The extract was washed with water and brine, dried (MgSO4), and conc. The residue was purified by chromatography with 10% ethyl acetate/cyclohexane to yield 5.6 g of methyl 2-(difluoromethyl)-5-(hydroxy-3-thienylmethyl)-4-(2-methylpropyl)-6-(trifluoromethyl)-3-pyridinecarboxylate, a 68.9% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05298479
Source datasetuspto-grants-1994_03
ORD IDord-cc71ec14a66f4742b7ca9541edec4a20
Source noteuspto-grants-1994_03