Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 129280Erstellt: 25. Oktober 2026

Water → HCID 22421025, Verbindung

https://huagongshe.com/reaction/129280

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktAcetyl chlorideHCID 6367—
EduktDimethyl 1,4-cyclohexanedicarboxylateHCID 7198—
EduktDiisopropylamineHCID 7912—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelHexaneHCID 8058—
ProduktHCID 22421025HCID 22421025—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

Di-isopropylamine (44.7 ml) was dissolved in dry tetrahydrofuran (400 ml) and cooled to -78° C. under nitrogen with mechanical stirring. A solution of B-butyllithium in hexane (1.6M, 197 ml) was added. After stirring at -78° C. for 10 minutes a solution of dimethyl cyclohexane-1,4-dicarboxylate (56.6 g, Lancaster) in tetrahydrofuran (200 ml) was added. After stirring for a further 30 minutes at -78° C. a solution of acetyl chloride (22.5 ml) in tetrahydrofuran (200 ml) was added. The reaction mixture was allowed to warm up to room temperature over a period of 3 hours. Water was then added and the mixture extracted with ether. The ethereal extracts were washed with water, saturated sodium bicarbonate solution, dilute hydrochloric acid and brine, and then were dried over anhydrous magnesium sulphate. Evaporation under reduced pressure gave a colourless oil which was slowly distilled to yield dimethyl 1-acetylcyclohexane-1,4-dicarboxylate (23.3 g, b.pt. 114°-120 C. at 0.4 mmHg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05466710
Quelldatensatzuspto-grants-1995_11
ORD IDord-7a01cc761f6a426c93cc4b606233d47c
Quellennotizuspto-grants-1995_11