HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57219Generated: October 25, 2026
Sodium Iodide → 4-Methylpentyl 5-(tetradecyloxy)furan-2-carboxylate
https://huagongshe.com/reaction/57219
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Pentane, 1-bromo-4-methyl- | HCID 69385 | — |
| Reactant | 5-(Tetradecyloxy)-2-furoic acid | HCID 115175 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 4-Methylpentyl 5-(tetradecyloxy)furan-2-carboxylate | HCID 66869812 | 62.2% |
Reaction Steps
To a vigorously stirred suspension of 5-(tetradecyloxy)furan-2-carboxylic acid (0.162 g, 0.5 mmol) in 10 mL of N,N-dimethylformamide was added 1-bromo-4-methylpentane (0.247 g, 1.5 mmol), cesium carbonate (0.243 g, 0.75 mmol) and sodium iodide (˜20 mg). The suspension appeared to go into solution briefly, and then a very finely dispersed white precipitate was observed. The reaction was allowed to stir for 12 hrs at which time HPLC analysis of the reaction solution indicated complete conversion of TOFA to a less polar product. The suspension was diluted with EtOAc (40 mL), brine (20 mL) and water (20 mL). The phases were separated and the organic phase was washed with water (20 mL) and brine (20 mL) and then dried and concentrated. The resulting crude material was purified by flash chromatography eluting with 0-20% EtOAc in hexanes to yield 0.127 g (62%) of the title compound. 1H NMR (300 MHz, CDCl3) δ: 7.15 (d, 1H), 5.30 (d, 1H), 4.22 (t, 2H), 4.10 (t, 2H), 1.18-1.80 (m, 29H), 0.89 (t, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09434718B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-06c8b30c5e0f4d0090984b9d5fe78529 |
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| Source note | uspto-grants-2016_09 |
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