Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1492839Generated: October 26, 2026

Potassium Iodide → HCID 15233477, compound

https://huagongshe.com/reaction/1492839

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(6-Bromohexyl)-2,3-bis(phenylmethoxy)benzeneHCID 14986434—
Reactant3-Hydroxy-5-(octadecyloxy)benzoic acid phenylmethyl esterHCID 15233476—
SolventAcetoneHCID 180—
SolventDimethylformamideHCID 6228—
ProductHCID 15233477HCID 1523347777%

Reaction Steps

A mixture of 1.5 g (3 mmol) of 3-hydroxy-5-(octadecyloxy) benzoic acid phenylmethyl ester, 1.6 g (3.4 mmol) of 1-(6-bromo-hexyl)-2,3-bis(phenylmethoxy)benzene [M. Carson, R.-J. Han and R. A. LeMahieu, U.S. Pat. No. 5,025,036 (1991)], 0.45 g (3 mmol) of potassium iodide and 0.84 g (6 mmol) of potassium carbonate in 40 ml of acetone and 10 ml of DMF was stirred at reflux for 47 hours. The solvents were removed at reduced pressure and the residue was purified by HPLC using 5% ethyl acetate-hexane to give 2.0 g (77% yield) of 3-[[6-[2,3-bis(phenylmethoxy)phenyl]hexyl]oxy]-5-(octadecyloxy)benzoic acid phenylmethyl ester as an oil. The nmr spectrum served to confirm the structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05374772
Source datasetuspto-grants-1994_12
ORD IDord-e4e2c8bbc33e4334ba63ac9ced579303
Source noteuspto-grants-1994_12