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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantCesium carbonateHCID 10796—
ReactantPentane, 1-bromo-4-methyl-HCID 69385—
Reactant5-(Tetradecyloxy)-2-furoic acidHCID 115175—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
SolventSodium chloride; waterHCID 57417360—
Product4-Methylpentyl 5-(tetradecyloxy)furan-2-carboxylateHCID 6686981262.2%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434718B2
Source datasetuspto-grants-2016_09
ORD IDord-06c8b30c5e0f4d0090984b9d5fe78529
Source noteuspto-grants-2016_09