Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 566426Erstellt: 25. Oktober 2026

Hydrochloric Acid → 6-(Hydroxymethyl)-N-(2-piperidinoethyl)-3-cyclohexene-1-carboxamide

https://huagongshe.com/reaction/566426

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktN-(2-Aminoethyl)piperidineHCID 33944—
EduktTetrahydrophthalic anhydride, cis-HCID 98495—
EduktSodium borohydrideHCID 4311764—
LösungsmittelWaterHCID 962—
LösungsmittelIsopropanolHCID 3776—
Produkt6-(Hydroxymethyl)-N-(2-piperidinoethyl)-3-cyclohexene-1-carboxamideHCID 21266117—

Reaktionsbedingungen

Temperatur140 °C

Reaktionsschritte

N-(2-Aminoethyl)piperidine (2.11 g) was added to cis-4-cyclohexene-1,2-dicarboxylic anhydride (2.50 g) and stirred for 6 hours at 140° C. The reaction mixture was suspended into a mixed solution of 2-propanol (125 ml) and water (21 ml) and then sodium borohydride (3.12 g) was added thereto at room temperature. After being stirred for 68 hours at room temperature, the reaction mixture was acidified with dilute hydrochloric acid and then concentrated. The residue was adjusted to pH 9 with saturated sodium hydrogencarbonate aqueous solution and 1N sodium hydroxide, and then extracted with ethyl acetate. The extract was washed with saturated brine, dried over sodium sulfate anhydride, and concentrated, thereby yielding a crude (3.34 g) containing the entitled compound as brown syrup.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06174885B1
Quelldatensatzuspto-grants-2001_01
ORD IDord-c1fd2ea043c24870adbe68e0b74e7971
Quellennotizuspto-grants-2001_01