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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1957928Generated: November 2, 2026

p-(Trifluoromethoxy)phenyl isocyanate → HCID 59363501, compound

https://huagongshe.com/reaction/1957928

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-(Trifluoromethoxy)phenyl isocyanateHCID 92298—
ReactantAmmonium formateHCID 2723923—
ReactantEthyl 1-methyl-4-nitro-1H-pyrrole-2-carboxylateHCID 10442704—
CatalystPalladiumHCID 23938—
SolventEthanol ethylacetateHCID 21584252—
ProductHCID 59363501HCID 59363501—

Reaction Conditions

Temperature80 °C

Reaction Steps

304 mg (1.53 mmol) of ethyl 1-methyl-4-nitro-1H-pyrrole-2-carboxylate are initially charged in 6 ml of ethyl acetate/ethanol (1:1), 163 mg (0.15 mmol) of palladium (10% on activated carbon) and 580 mg (9.20 mmol) of ammonium formate are added, and the mixture is stirred at 80° C. for 1 h. After cooling, the mixture is filtered through kieselguhr, the filtercake is rinsed with ethanol and the filtrate is freed from the solvent under reduced pressure. The residue is dissolved in 6 ml of THF, 374 mg (1.84 mmol) of 4-trifluoromethoxyphenyl isocyanate are added and the mixture is stirred at RT for 1 h. The reaction solution is concentrated and the residue is purified by RP-HPLC (acetonitrile/water). This gives a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410090B2
Source datasetuspto-grants-2013_04
ORD IDord-e5518b05fa734e4398a821c115047757
Source noteuspto-grants-2013_04