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HRID 42732作成日:2026年10月25日

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

https://huagongshe.com/reaction/42732

反応式

関与物質

役割名称HCID仕込み量
反応物AcetonitrileHCID 6342—
反応物2-(Carboxymethoxy)thioxanthoneHCID 3019853—
反応物4-Hydroxybutylacrylate glycidyletherHCID 22323150—
触媒2,6-Di-tert-butyl-4-methylphenolHCID 31404—
触媒Tetrabutylammonium BromideHCID 74236—
溶媒DimethylacetamideHCID 31374—
生成物acrylic acid 4-{2-hydroxy-3-[2-(9-oxo-9H-thioxanthen-2-yloxy)-acetoxy]-propoxy}-butyl esterHCID 58325515144.2%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08536217B2
出典データセットuspto-grants-2013_09
ORD IDord-0d06cbb7a63845c398af753e17c01870
出典メモuspto-grants-2013_09