HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1655477Generated: October 30, 2026
2-Ethylhexanoic Acid → HCID 178441466, compound
https://huagongshe.com/reaction/1655477
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Ethylhexanoic Acid | HCID 8697 | — |
| Reactant | Azido(trimethyl)stannane | HCID 5104973 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 19792117 | HCID 19792117 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178441466 | HCID 178441466 | 31% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05250554 |
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| Source dataset | uspto-grants-1993_10 |
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| ORD ID | ord-3d798e8655b04152a12624ea521ecca2 |
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| Source note | uspto-grants-1993_10 |
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