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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1110246Generated: October 27, 2026

Sodium Iodide → 3-(Octadecyloxy)-5-(3-phenoxypropoxy)benzoic acid phenylmethyl ester

https://huagongshe.com/reaction/1110246

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
ReactantBenzene, (3-bromopropoxy)-HCID 68522—
Reactant3-Hydroxy-5-(octadecyloxy)benzoic acid phenylmethyl esterHCID 15233476—
SolventAcetoneHCID 180—
SolventDimethylformamideHCID 6228—
Product3-(Octadecyloxy)-5-(3-phenoxypropoxy)benzoic acid phenylmethyl esterHCID 1523283396%

Reaction Steps

A mixture of 12 g (0.024 mol) of 3-hydroxy-5-(octadecyloxy)benzoic acid phenylmethyl ester, 6 ml (0.038 ml) of 3-phenoxypropyl bromide, 3.6 g (0.024 mol) of sodium iodide and 10 g (0.072 mol) of potassium carbonate in 40 ml of acetone and 80 ml of DMF was stirred at reflux for 46 hours. The reaction mixture was filtered and the filtrate was concentrated to dryness at reduced pressure. Water was added to the residue and the product was extracted with ethyl acetate. The dried extract was concentrated at reduced pressure to an oil which was purified by HPLC using 5% ethyl acetate-hexane. The pure fractions were combined, triturated with hexane and filtered to give 14.6 g (96% yield, mp 46°-47°) of 3-(octadecyloxy)-5-(3-phenoxypropoxy)benzoic acid phenylmethyl ester. The structure was confirmed by nmr and mass spectra.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05324747
Source datasetuspto-grants-1994_06
ORD IDord-71255de257a34b789d3b3a763a2c6cb9
Source noteuspto-grants-1994_06