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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 42732Generated: October 25, 2026

Acetonitrile → acrylic acid 4-{2-hydroxy-3-[2-(9-oxo-9H-thioxanthen-2-yloxy)-acetoxy]-propoxy}-butyl ester

https://huagongshe.com/reaction/42732

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
Reactant2-(Carboxymethoxy)thioxanthoneHCID 3019853—
Reactant4-Hydroxybutylacrylate glycidyletherHCID 22323150—
Catalyst2,6-Di-tert-butyl-4-methylphenolHCID 31404—
CatalystTetrabutylammonium BromideHCID 74236—
SolventDimethylacetamideHCID 31374—
Productacrylic acid 4-{2-hydroxy-3-[2-(9-oxo-9H-thioxanthen-2-yloxy)-acetoxy]-propoxy}-butyl esterHCID 58325515144.2%

Reaction Steps

A reaction mixture containing (9-oxo-9H-thioxanthen-2-yloxy)acetic acid (4.0 g, 14 mmol), acetonitrile (55 ml), dimethylacetamide (10 mL), tetrabutylammonium bromide (0.5 g, 1.4 mmol) and 2,6-di-tert-butyl-4-methylphenol (0.03 g, 0.114 mmol) was heated to reflux. At this temperature 4-hydroxybutylacrylate glycidylether (2.3 g, 11.4 mmol) was added and the mixture was allowed to stir at reflux temperature for 16 hours. The mixture was cooled to room temperature and the solvent was evaporated under reduced pressure to provide 8.0 g of a yellow oil. The product was purified on a Prochrom LC80 Column using Kromasil Si 60A 10 μm as silica and dichloromethane/ethyl acetate (60/40) as eluent, to afford 1.8 g of a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536217B2
Source datasetuspto-grants-2013_09
ORD IDord-0d06cbb7a63845c398af753e17c01870
Source noteuspto-grants-2013_09