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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1576017Erstellt: 25. Oktober 2026

Hydroquinone → 3-(4-Chlorophenyl)-7-[(4-chlorophenyl)methylene]-2,3,3a,4,6,7-hexahydro-2-propylthiopyrano[4,3-c]pyrazole

https://huagongshe.com/reaction/1576017

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydroquinoneHCID 785—
EduktHydrazine, propyl-HCID 42007—
Edukt4H-Thiopyran-4-one, 3,5-bis[(4-chlorophenyl)methylene]tetrahydro-HCID 382469—
Lösungsmittel1,1-DichloroethaneHCID 6365—
Produkt3-(4-Chlorophenyl)-7-[(4-chlorophenyl)methylene]-2,3,3a,4,6,7-hexahydro-2-propylthiopyrano[4,3-c]pyrazoleHCID 5365048940,4%

Reaktionsschritte

A mixture of 6.0g of tetrahydro-3,5-bis-[(4-chlorophenyl)methylene]-4H-thiopyran-4-one, 1.3g of n-propyl hydrazine, and 100mg of hydroquinone in 100ml of dichloroethane is heated at reflux temperature for 2.5 hours and allowed to cool to room temperature. The reaction mixture is washed with dilute hydrochloric acid and water, and then dried over calcium chloride. After the solvent is removed in vacuo, the residue is chromatographed on a dry packed neutral alumina column (Activity I). The fractions eluted with 0-5% ethyl acetate/hexane are combined and crystallized from acetone/acetonitrile to give 2.8g of the title compound, melting point 118°-122°C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS03979381
Quelldatensatzuspto-grants-1976_09
ORD IDord-b7b880a812034aebbe379598b6672279
Quellennotizuspto-grants-1976_09