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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767583Generated: October 30, 2026

2-Nitroaniline → 2-Nitrophenyl isocyanate

https://huagongshe.com/reaction/1767583

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-NitroanilineHCID 6946—
ReactantDiphosgeneHCID 10426—
SolventEthyl AcetateHCID 8857—
Product2-Nitrophenyl isocyanateHCID 76834—

Reaction Steps

Method a (from 2-nitroanilines): To a solution of diphosgene (4.1 mL, 34.1 mmol) in EtOAc (40 mL) at 0° C. was added a solution of the 2-nitroaniline (45.5 mmol) in EtOAc (200–500 mL), and the mixture was heated to reflux for 18 h. The solvent was removed in vacuum to leave a brown solid, which was triturated with hot hexane (200 mL). The solid material was filtered off and the filtrate was concentrated under reduced pressure to leave the pure 2-nitrophenylisocyanate as a yellow solid. This material was refluxed in a mixture of excess tert-BuOH in CH2Cl2 for 2.5 h. Removal of the solvent left an orange solid which was purified by silica gel column chromatography with hexane/EtOAc to give the (2-nitro-phenyl)-carbamic acid tert-butyl ester as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07235547B2
Source datasetuspto-grants-2007_06
ORD IDord-cbb03a853ce048c0a44d745a629013e3
Source noteuspto-grants-2007_06