Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 899421Generated: October 26, 2026

Hydrochloric Acid → 2-(Carboxymethoxy)thioxanthone

https://huagongshe.com/reaction/899421

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium HydroxideHCID 14798—
ReactantSodiumHCID 5360545—
Reactant2-Hydroxy-9H-thioxanthen-9-oneHCID 9794568—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-(Carboxymethoxy)thioxanthoneHCID 3019853—

Reaction Steps

24 g sodium hydroxide was refluxed in 400 ml tetrahydrofuran for five minutes. 22.8 g (0.1 mols) 2-hydroxythioxanthone was added and reflux was continued for 1 hour, during which time the colour changed to bright red, indicating the formation of the sodium salt of 2-hydroxythioxanthone. 35.1 g (0.21 mols) of ethyl bromoacetate was added and reflux was continued for three hours. After cooling to room temperature, 400 ml of deionised water was added, with stirring, and the tetrahydrofuran was distilled out to yield a clear red solution. Reflux was continued for a further 2 hours in order to hydrolyse all the ester intermediate. The solution was then cooled to 50° C., and 400 ml 1.0 M hydrochloric acid was added, with stirring, causing the solid product to precipitate out. After refluxing for a further five minutes to be sure that all the sodium salt was converted to free acid, the solution was cooled to room temperature and stirred for two hours before filtering off the solid, washing with 400 ml deionised water and drying in a vacuum oven at 80° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07354957B2
Source datasetuspto-grants-2008_04
ORD IDord-98502927409346a2b432102c6d631c00
Source noteuspto-grants-2008_04