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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-(Trifluoromethoxy)phenyl isocyanate | HCID 92298 | — |
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | Ethyl 1-methyl-4-nitro-1H-pyrrole-2-carboxylate | HCID 10442704 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol ethylacetate | HCID 21584252 | — |
| Product | HCID 59363501 | HCID 59363501 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08410090B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-e5518b05fa734e4398a821c115047757 |
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| Source note | uspto-grants-2013_04 |
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