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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 21851Erstellt: 23. Oktober 2026

Hydrochloric Acid → Phenyl chloroformate

https://huagongshe.com/de/reaction/21851

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktPhenolHCID 996—
EduktPhosgeneHCID 6371—
EduktSodium HydroxideHCID 14798—
EduktPhosgene phenolHCID 86748739—
KatalysatorTriphenyl phosphiteHCID 7540—
ProduktPhenyl chloroformateHCID 1589196,3%

Reaktionsbedingungen

Temperatur140 °C

Reaktionsschritte

A four-necked flask equipped with a gas inlet, a dry ice condenser, a mechanical stirrer, a thermocouple and a sampling port is charged with phenol (Aldrich, 287.5 g, 2.907 mol) and triphenyl phosphite (10.12 g, 32.61 mmol). The temperature is raised to 140° C. and phosgene (274 g, 2.77 mol) is added over a 465 minute period. Phosgene/phenol molar ratio is 0.95. A recirculating aqueous sodium hydroxide scrubber is used to neutralize the coproduct hydrochloric acid and to destroy traces of phosgene which are not condensed in the condenser. After the phosgene addition is stopped, a nitrogen stream is used to purge residual phosgene and the reactor is cooled to ambient temperature. The colorless crude product is isolated by vacuum distillation to give phenyl chloroformate (417.84 g, bp 73°-77° C. at 14 mm Hg) containing 6.6 percent by weight residual phenol. Selectivity to phenyl chloroformate is 95 mole percent based on phenol, 90 mole percent based on phosgene.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05424473
Quelldatensatzuspto-grants-1995_06
ORD IDord-a0df9aa2b5d94cfb8738aba40dd8ebff
Quellennotizuspto-grants-1995_06