Реакция #412622

ord-9080267a457240da87884a2010723a7e

Уравнение реакции

O=C1OC(=O)C2C3C=CC(O3)C12
anhydride
O=C1OC(=O)C2C3C=CC(O3)C12
7-oxabicyclo [2.2.1]hept-2-ene-5,6-dicarboxylic acid anhydride
C=CC(=O)OCCO
2-hydroxyethyl acrylate
C=CC(=O)OCCOC(=O)C1C2C=CC(O2)C1C(=O)O
desired compound
C=CC(=O)OCCOC(=O)C1C2C=CC(O2)C1C(=O)O
2-(Acryloyloxy)ethyl 5-carboxy-7-oxabicyclo [2.2.1]hept-2-ene-6-carboxylate

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.DISTILLATIONthe toluene was distilled off under reduced pressure

Методика

Maleic anhydride (50 g) and furan (150 ml) were heated under reflux for 1 hour, and then the excess of furan was distilled off. The residue was recrystallised from chloroform, yielding 72 g of 7-oxabicyclo [2.2.1]hept-2-ene-5,6-dicarboxylic acid anhydride (m.pt. 110° C., decomp.). This anhydride (40 g) and 30.75 g of 2-hydroxyethyl acrylate were heated in 250 ml of toluene at 100° C. for 3 hours, and then the toluene was distilled off under reduced pressure, leaving the desired compound as a viscous liquid.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04440850uspto-grants-1984_04