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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1655477Generated: October 30, 2026

2-Ethylhexanoic Acid → HCID 178441466, compound

https://huagongshe.com/reaction/1655477

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Ethylhexanoic AcidHCID 8697—
ReactantAzido(trimethyl)stannaneHCID 5104973—
ReactantSodiumHCID 5360545—
ReactantHCID 19792117HCID 19792117—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 178441466HCID 17844146631%

Reaction Steps

A mixture of 2-butyl-1-[(2'-cyanobiphenyl-4-yl)methyl]- 7-methoxymethylbenzimidazole (0.6 g) and trimethyltin azide (1.2 g) in toluene (12 ml) was heated for 3 days under reflux in toluene (12 ml). The solvent was distilled off. To the residue was added 1N-HCl (8 ml) and the mixture was stirred for a while, followed by extraction with ethyl acetate. The organic layer was washed with water and dried, then the solvent was distilled off. The residue was purified by column chromatography on silica gel to give an oil. The product was dissolved in ethyl acetate, to which was added a methanol solution of sodium salt of 2-ethyl hexanoic acid (0.25 g). The mixture was concentrated. Crystals separated out were recrystallized from toluene --ethyl acetate to afford colorless crystals (0.22 g, 31%), m.p.175-178° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05250554
Source datasetuspto-grants-1993_10
ORD IDord-3d798e8655b04152a12624ea521ecca2
Source noteuspto-grants-1993_10