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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1248184Erstellt: 25. Oktober 2026

1,4-Dichloro-2-butene, (2E)- → 1-Phenylsulfonyl-1-acetyl-2-vinylcyclopropane

https://huagongshe.com/reaction/1248184

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,4-Dichloro-2-butene, (2E)-HCID 642197—
EduktPhenylsulfonylacetoneHCID 735827—
Produkt1-Phenylsulfonyl-1-acetyl-2-vinylcyclopropaneHCID 15592219—

Reaktionsschritte

Utilizing a phase-transfer procedure similar to that described in Example I, phenylsulfonylacetone was reacted with 1,4-dichlorobutene-2 to obtain 1-phenylsulfonyl-1-acetyl-2-vinylcyclopropane. For the reaction, 9.91 grams phenylsulfonylacetone (Parish Chemical Co.) and 6.25 grams 1,4-dichlorobutene-2 were combined in 20 mls sulfolane containing 6.6 grams potassium hydroxide (85%) and 5 mole percent tricaprylylmethylammonium chloride. The reaction mixture was stirred at 35°-40° C. for 31/2 hours. One-hundred mls water was then added to dissolve the white granular precipitate which had formed and the mixture extracted several times with ether. A crude red oil (10.8 grams) was obtained after removal of the ether and further work-up utilizing a Waters Preparatory Liquid Chromatograph 500A equipped with a gel permeation column and operated at a flow rate of 0.1 l/min yielded the cis and trans isomers of 1-phenylsulfonyl-1-acetyl-2-vinylcyclopropane. ##STR18## trans 1-phenylsulfonyl-1-acetyl-2-vinylcyclopropane

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04522950
Quelldatensatzuspto-grants-1985_06
ORD IDord-751477902f794577865dca0d090f3ea1
Quellennotizuspto-grants-1985_06