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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1165167Generated: October 26, 2026

Deferiprone → 3-(n-octanoyloxy)-1,2-dimethyl-4-(1H)-pyridinone

https://huagongshe.com/reaction/1165167

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDeferiproneHCID 2972—
ReactantOctanoyl chlorideHCID 8124—
ReactantTriethylamineHCID 8471—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
Product3-(n-octanoyloxy)-1,2-dimethyl-4-(1H)-pyridinoneHCID 19862588—

Reaction Steps

With stirring, 0.56 ml of triethylamine is added at room temperature to a suspension of 0.556 g of 3-hydroxy-1,2-dimethyl-4(1H)-pyridinone in 40 ml of acetonitrile and 40 ml of methylene chloride, followed by the addition of 1.02 ml of caprylyl chloride. A solution forms within 3 minutes and after 30 minutes the reaction is complete, and the volatile constituents are removed by evaporation under reduced pressure. The residue is dried under a high vacuum and crystallised from a mixture of methylene chloride and ethyl acetate. The 3-(n-octanoyloxy)-1,2-dimethyl-4-(1H)-pyridinone so obtained begins to sinter at 140° C. and decomposes at 180° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04908371
Source datasetuspto-grants-1990_03
ORD IDord-0b42757bf86e4eb58e5a4fb473db2d72
Source noteuspto-grants-1990_03