HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 376857Generated: October 31, 2026
Hydrochloric Acid → 2,6-Difluorobenzoyl isocyanate
https://huagongshe.com/reaction/376857
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 2,6-Difluorobenzamide | HCID 87439 | — |
| Reactant | Isocyanate | HCID 105034 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 2,6-Difluorobenzoyl isocyanate | HCID 2733369 | — |
Reaction Steps
In order to synthesize the isocyanate, 1.57 g (10 mmol) of 2,6-difluorobenzamide and 15 ml of dry 1,2-dichloroethane were introduced into a 100 ml flask and then 0.92 g (10.5 mmol) of oxalyl chloride was slowly added thereto at normal temperature by means of a syringe, during which an exothermic reaction occurred that generated hydrochloride gas. The resulting reaction mixture was refluxed for 5 hours and cooled to normal temperature. The reaction solvent and the excess oxalyl chloride were removed therefrom under vacuo to obtain 2,6-difluorobenzoyl isocyanate in an oily state. Thus obtained 2,6-difluorobenzoyl isocyanate was then dissolved in 20 ml of dry 1,2-dichloroethane. Then, 2.63 g of 2-chloro-3,5-bis(trifluoromethyl)aniline was added thereto, reacted for 3 hours, and filtered to obtain 4.15 g (Yield from benzamide, 93%) of the title compound as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06022882 |
|---|
| Source dataset | uspto-grants-2000_02 |
|---|
| ORD ID | ord-c94d970e9a6e47519ec71e9a98559b60 |
|---|
| Source note | uspto-grants-2000_02 |
|---|