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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 5974Erstellt: 23. Oktober 2026

Water → Dimethyl 3-bromocyclobutane-1,2-dicarboxylate

https://huagongshe.com/de/reaction/5974

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktAcetophenoneHCID 7410—
EduktMaleic AnhydrideHCID 7923—
EduktEthyl AcetateHCID 8857—
EduktBromoetheneHCID 11641—
ProduktDimethyl 3-bromocyclobutane-1,2-dicarboxylateHCID 1979425719,5%

Reaktionsschritte

A solution of 5 g (51 mmol) of maleic anhydride and 0.5 mL (4 mmol) of acetophenone in 50 mL of ethyl acetate was added to a 100 mL pyrex photochemical reaction vessel. The vessel was sealed and purged with nitrogen for 10 min then cooled with tap water while 13.8 g (129 mmol) of vinyl bromide was being added to the ethyl acetate solution. The vessel was then irradiated for 20 h with a 450 Watt medium pressure mercury vapor lamp. The solution was concentrated in vacuo and the residue dissolved in 200 mL of methanol which had been treated with 1 mL of trimethylsilyl chloride. The solution was stirred at ambient temperature overnight and then concentrated to a brown viscous oil. The oil was chromatographed on silica gel (200 g) eluted with 20% ethyl acetate in hexane to give a yellow oil. The oil was purified by short-path distillation using a 1" fractionating column to give 2.5 g (19.5% yield) of the title compound; b.p. 75°-80° C. (0.1 mm Hg); EI-MS, m/e (rel intensity): 220 (M+ --CH3O, 60), 218 (60), 192 (42), 190 (39), 171 (100); 1H NMR (CDCl3) δ2.60 (m, 1H), 2.82 (m, 1H), 3.56 (td, 1H), 3.72 (m, 6H), 3.94 (t, 0.4H), 4.12 (q, 0.6H), 4.93 (q, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05246931
Quelldatensatzuspto-grants-1993_09
ORD IDord-ba400473a2ca4271ac076e19bab41291
Quellennotizuspto-grants-1993_09