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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 554714Generated: October 31, 2026

4-Chlorophenyl Isocyanate → 4-bromo-N-(2,2,2-trichloro-1-(4-chlorophenylamino)ethyl)furan-2-carboxamide

https://huagongshe.com/reaction/554714

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorophenyl IsocyanateHCID 7693—
Reactant4-bromo-N-(2,2,2-trichloro-1-hydroxyethyl)furan-2-carboxamideHCID 58149535—
CatalystTriethylamineHCID 8471—
SolventBenzeneHCID 241—
Product4-bromo-N-(2,2,2-trichloro-1-(4-chlorophenylamino)ethyl)furan-2-carboxamideHCID 44814646—

Reaction Steps

was prepared in accordance with reported methods: see Ulrich, H. et al J Org. Chem., 33, 1968, 2887. A solution of 4-bromo-N-(2,2,2-trichloro-1-hydroxyethyl)furan-2-carboxamide (preparation as for 6 above) (0.566 g, 1.67 mmol), 1-chloro-4-isocyanato-benzene (0.264 g, 1.68 mmol) and triethylamine (2 drops) in benzene (4 mL) was heated at 95° C. for 1.5 h. The mixture was evaporated under reduced pressure. The residue was solvated with chloroform and concentrated onto silica gel. Chromatographic purification on an auto-column with 30% dichloromethane in hexanes gave 4-bromo-N-(2,2,2-trichloro-1-(4-chlorophenylamino)ethyl)furan-2-carboxamide (Compound 33) as a white solid; 422 mg (57%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08049037B2
Source datasetuspto-grants-2011_11
ORD IDord-400d02ae3a6c4241a05bea9857716e06
Source noteuspto-grants-2011_11