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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30511Generated: October 30, 2026

Oxygen → Phenyl isocyanate

https://huagongshe.com/reaction/30511

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxygenHCID 977—
ReactantSodium IodideHCID 5238—
ReactantAnilineHCID 6115—
Reactant2,2,2-TrifluoroethanolHCID 6409—
ReactantHCID 178418416HCID 178418416—
Solvent1,2-DichlorobenzeneHCID 7239—
ProductPhenyl isocyanateHCID 7672—

Reaction Conditions

Temperature120 °C

Reaction Steps

In a 1000 ml high-pressure stirred autoclave 15.5 g of aniline, 7.6 g of the [Co-tBu-Salen]/Silica catalyst of Example 2, 1.78 g of NaI and 488 g of 2,2,2-trifluoroethanol (TFE) are charged. The autoclave is pressurized with carbon monoxide and oxygen in a volumetric ratio of 19/1. The temperature is increased to 120° C. and the total pressure is maintained constant at 40 bars. The reaction is maintained under constant vigorous stirring for three hours. After 3 hours the reactor is cooled to room temperature, depressurized and 97.8 g of 1,2-dichlorobenzene (DCB) is charged in the reactor. The temperature is increased to 180° C. under atmospheric pressure. The vapors of TFE are separated, condensed, and reused in the following example. In the bottom of the reactor a mixture of DCB and phenylisocyanate is obtained. From this mixture pheylisocyanate is recovered by distillation with 99% w/w purity.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07423171B2
Source datasetuspto-grants-2008_09
ORD IDord-663207ea753249b2b73ea398f8b834d2
Source noteuspto-grants-2008_09