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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131673Generated: October 30, 2026

Phenyl isocyanate → HCID 47448403, compound

https://huagongshe.com/reaction/131673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl isocyanateHCID 7672—
ReactantTriethylamineHCID 8471—
ReactantHCID 86760687HCID 86760687—
SolventEthanolHCID 702—
ProductHCID 47448403HCID 4744840395.8%

Reaction Steps

N-(3-Nitrobenzyl)-N′-phenylurea 3-Nitrobenzylamine hydrochloride (377 mg, 2.0 mmol) and triethylamine (278 μl, 2 mmol) were stirred in ethanol (5 ml) for 15 min. Phenylisocyanate (230 μl, 2.12 mmol) was added dropwise to the solution and stirring continued for 45 min at room temperature once the addition was complete. The reaction was concentrated under vacuum and the residue partitioned between ethyl acetate and water. The organic phase was washed with water, dried (sodium sulphate) and the solvent evaporated under vacuum to give N-(3-nitrobenzyl)-N′-phenylurea (520 mg). MP; 153-156° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07384963B2
Source datasetuspto-grants-2008_06
ORD IDord-f6679c34ee5f4cbca2bee3a8c1c4342b
Source noteuspto-grants-2008_06