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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 279910Erstellt: 25. Oktober 2026

Pyridine → HCID 54422056, Verbindung

https://huagongshe.com/reaction/279910

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktTriclosanHCID 5564—
EduktThionyl ChlorideHCID 24386—
Edukt2-Hexadecanoyloxy-1-(hexadecanoyloxymethyl)ethyl hydrogen glutarateHCID 23322903—
LösungsmittelCyclohexaneHCID 8078—
ProduktHCID 54422056HCID 54422056—

Reaktionsbedingungen

Temperatur35 °C

Reaktionsschritte

A mixture of cyclohexane (60 ml.), pyridine (1.43 ml.) and 2-hexadecanoyloxy-1-(hexadecanoyloxymethyl)ethyl hydrogen glutarate (B) (11.0 g.) was warmed to 35° C. The solution obtained was added dropwise during 45 minutes to a stirred solution of thionyl chloride (1.23 ml.) in cyclohexane (25 ml.) at 35° C. The mixture was then stirred for a further 1.5 hours at 35° C., cooled to 15° C. and a solution of triclosan (4.68 g.) and pyridine (1.56 ml.) in cyclohexane (20 ml.) added during 15 minutes. The mixture was stirred at ambient temperature for 16 hours, warmed to 35° C. and washed first with 0.5 M hydrochloric acid (100 ml.) and then with water (3×100 ml.), also heated to 35° C. The mixture was then dried (MgSO4) and evaporated to give 5-chloro-2-(2,4-dichlorophenoxy)phenyl 2-hexadecanoyloxy-1-(hexadecanoyloxymethyl)ethyl glutarate as a white solid, m.p. 44°-46° C., identical with the material obtained in Example 4 as judged by its NMR and mass spectral properties.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04587262
Quelldatensatzuspto-grants-1986_05
ORD IDord-b9c7435022e044fba33b4ced42b2f2cc
Quellennotizuspto-grants-1986_05