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HRID 385200Erstellt: 24. Oktober 2026

Dimethyl 2-chloroterephthalate → Dimethyl 2-chloro-cyclohexane-1,4-dicarboxylate

https://huagongshe.com/de/reaction/385200

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl 2-chloroterephthalateHCID 87740—
EduktDimethyl muconate, (E,E)-HCID 5370244—
KatalysatorPalladiumHCID 23938—
LösungsmittelDimethyldipropyleneglycolHCID 86648893—
ProduktDimethyl 2-chloro-cyclohexane-1,4-dicarboxylateHCID 66809701—

Reaktionsbedingungen

Temperatur165 °C

Reaktionsschritte

In a Parr pressure reactor, a stirred suspension of trans,trans dimethyl muconate (6.1 g, 36 mmol) in dimethyldipropyleneglycol (120 ml, 0.3 M) is heated under vinyl chloride pressure (18 psi (0.124 MPa) at 23° C.) to 165° C. for 48 hours. After cooling to room temperature, the reaction mixture is diluted using the same solvent to 200 ml in a volumetric flask, transferred into a round-bottom flask equipped with a magnetic stirring bar, and Pd/C catalyst is added (360 mg of Johnson-Matthey 5 percent Pd/C #6, 0.2 mol percent) at room temperature. The flask is equipped with a reflux condenser, flitted gas dispersion tube, and internal T probe. Under N2 flow (190 ml/min) and stirring (190 rpm) the mixture is heated to reflux while samples are taken at appropriate intervals (t=0.0, 0.25, 0.5, 1.0, 2.0, 4.0, 8.0 h) to monitor the progress of the reactions occurring. After 8 hour reaction time, dimethyl chloro-terephthalate is present. Some material also undergoes C—Cl bond cleavage and dimethyl 2-chloro-cyclohexane-1,4-dicarboxylate is also formed.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08367858B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-48293e6836224ac38b538d3c5b15e108
Quellennotizuspto-grants-2013_02