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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256809Generated: October 28, 2026

Hydrochloric Acid → HCID 22668864, compound

https://huagongshe.com/reaction/256809

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantFuranHCID 8029—
ReactantMethyl 2-(difluoromethyl)-5-formyl-4-(2-methylpropyl)6-(trifluoromethyl)-3-pyridinecarboxylateHCID 15107640—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
ProductHCID 22668864HCID 2266886461.4%

Reaction Conditions

Temperature-6 °C

Reaction Steps

To 2.5N n-BuLi in hexane (30 mL) cooled to 0 ° C was added in a slow stream furan (7 g, 0.1 mol) in anhydrous ether (60 mL). The mixture was heated at reflux for 3 h under a nitrogen atmosphere and then cooled to -6° C. A solution of methyl 2-(difluoromethyl)-5-formyl-4-(2-methylpropyl)-6-(trifluoromethyl)-3-pyridinecarboxylate (6 g, 17.6 mmol) in anhydrous ether (20 mL) was added dropwise and stirring was continued for 2 h. The mixture was 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 oily residue was purified by chromatography with 10% ethyl acetate/cyclohexane to yield 4.4 g of methyl 2-(difluoromethyl)-5-(2-furanylhydroxymethyl)-4-(2-methylpropyl)-6-(trifluoromethyl)-3-pyridinecarboxylate as an orange oil, a 61% yield. nD25 1.4863.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05260262
Source datasetuspto-grants-1993_11
ORD IDord-f9b4a091784f47e08799e62c04fe7610
Source noteuspto-grants-1993_11