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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1492107Generated: October 25, 2026

2,4,6-Triiodophenol → 2,4,6-Triiodophenyl (2-propyl)pentanoate

https://huagongshe.com/reaction/1492107

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4,6-TriiodophenolHCID 11862—
Reactant2-Propylvaleryl chlorideHCID 76240—
ReactantSodium BicarbonateHCID 516892—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventAcetonitrileHCID 6342—
Product2,4,6-Triiodophenyl (2-propyl)pentanoateHCID 8674789268%

Reaction Steps

A mixture of 2,4,6-triiodophenol (2.0 g, 4.24 mmol), 2-propylvaleroyl chloride (2.5 ml, 12.7 mmol, 3 eq) and 4-dimethylaminopyridine (DMAP; 20 mg) in 20 ml of acetonitrile was refluxed under argon overnite. The reaction mixture was cooled and poured into excess aqueous sodium bicarbonate and then extracted with dichloromethane. The dichloromethane extract was dried over magnesium sulfate, filtered, and evaporated to give the crude product (2.42 mmol, 95%) as a pink solid. Recrystallization from ethyl acetate gave 1.75 g (68%) of pure product, mp 99°-101° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05372800
Source datasetuspto-grants-1994_12
ORD IDord-5486c657423046cd92e9863ba2b03e93
Source noteuspto-grants-1994_12