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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 42732생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/42732

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물2-(Carboxymethoxy)thioxanthoneHCID 3019853—
반응물4-Hydroxybutylacrylate glycidyletherHCID 22323150—
촉매2,6-Di-tert-butyl-4-methylphenolHCID 31404—
촉매Tetrabutylammonium BromideHCID 74236—
용매DimethylacetamideHCID 31374—
생성물acrylic acid 4-{2-hydroxy-3-[2-(9-oxo-9H-thioxanthen-2-yloxy)-acetoxy]-propoxy}-butyl esterHCID 58325515144.2%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536217B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-0d06cbb7a63845c398af753e17c01870
출처 메모uspto-grants-2013_09