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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488257Generated: October 27, 2026

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

https://huagongshe.com/reaction/488257

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 1523283396.4%

Reaction Steps

A mixture of 12 g (0.024 mol) of 3-hydroxy-5-(octadecyloxy)benzoic acid phenylmethyl ester, 6 ml (0.038 mol) of 3-phenoxypropyl bromide, 3.6 g (0.024 mol) of sodium iodide and 10 g (0.072 mol) of potassium carbonate in 400 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 numberUS05298652
Source datasetuspto-grants-1994_03
ORD IDord-e3349e6c12f2490fa57e84acde8e6ec1
Source noteuspto-grants-1994_03