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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 64775Erstellt: 23. Oktober 2026

Sulfuric Acid → 3-Penten-2-one, 3-methyl-5-(2,2,3-trimethyl-3-cyclopenten-1-yl)-

https://huagongshe.com/de/reaction/64775

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
EduktMethyl Ethyl KetoneHCID 6569—
EduktPotassium HydroxideHCID 14797—
Edukt3-Cyclopentene-1-acetaldehyde, 2,2,3-trimethyl-HCID 98497—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
Produkt3-Penten-2-one, 3-methyl-5-(2,2,3-trimethyl-3-cyclopenten-1-yl)-HCID 643696960,4%

Reaktionsschritte

152 G (1.0 M) of campholenic aldehyde having a purity of about 75% were added dropwise under stirring in 15-20 minutes to a mixture cooled at -5/-10° of 400 g (6.1 M) of methyl-ethyl ketone, 1025 g (35 M) of methanol, 30.5 g (0.54 M) of potassium hydroxide and 380 g of water. The mixture was kept at -5° for 24 hours, then at room temperature for the same period and neutralized thereupon with H2SO4 to 62.5%. After concentration under reduced pressure, the obtained residue was dissolved in 200 ml of water, diluted with petrol ether 30/50, washed until neutrality, dried and concentrated. 189.3 G of a raw material was thus obtained which on distillation with a Vigreux column of 15 cm length gave 144.6 g of (E)-3-methyl-5-(2,2,3-trimethyl-3-cyclopenten-1-yl)-3-penten-2-one having a purity of 86% (yield 60.4%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04610813
Quelldatensatzuspto-grants-1986_09
ORD IDord-2df230ea3a7f4123889382b5a88a7f02
Quellennotizuspto-grants-1986_09