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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004864Generated: October 30, 2026

2,6-Dichlorobenzamide → 2,6-Dichlorobenzoyl isocyanate

https://huagongshe.com/reaction/1004864

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-DichlorobenzamideHCID 16183—
ReactantOxalyl chlorideHCID 65578—
Solvent1,2-DichloroethaneHCID 11—
Product2,6-Dichlorobenzoyl isocyanateHCID 12912739—

Reaction Conditions

Temperature100 °C

Reaction Steps

0.51 g (2.7 mmol) of 2,6-dichlorobenzamide and 0.41 g (3.2 mmol, 1.2 eq) of oxalyl chloride were added to 10 ml of 1,2-dichloroethane and then the mixture was stirred for 8 hours at 100° C. The reaction solution was cooled down to room temperature. The reaction solvent and excessive oxalyl chloride were removed by distillation under reduced pressure to obtain 2,6-dichlorobenzoyl isocyanate in an oily state. 10 ml of fresh 1,2-dichloroethane and 0.86 g (2.7 mmol) of 4,5-dibromo-2-trifluoromethyl aniline were successively added thereto, reacted for 2 hours and filtered to obtain 0.28 g (Yield 43%) of the title compound as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06051737
Source datasetuspto-grants-2000_04
ORD IDord-610b37c7d0ac4cceb3d8674386a021bf
Source noteuspto-grants-2000_04