HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004870Generated: October 31, 2026
Oxalyl chloride → 2-Fluorobenzoyl isocyanate
https://huagongshe.com/reaction/1004870
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 2-Fluorobenzamide | HCID 67964 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 2-Fluorobenzoyl isocyanate | HCID 13080392 | — |
Reaction Steps
0.38 g (2.7 mmol) of 2-fluorobenzamide and 0.36 g (2.9 mmol, 1.1 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-fluorobenzoyl isocyanate in an oily state. 10 ml of fresh 1,2-dichloroethane and 0.7 g (2.7 mmol) of 2-bromo-4-fluoro-5-trifluoromethyl aniline were successively added thereto, reacted for 2 hours and filtered to obtain 1.06 g (Yield 93%) of the title compound as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06051737 |
|---|
| Source dataset | uspto-grants-2000_04 |
|---|
| ORD ID | ord-6e8f19bceeb94675af6bdee7a0774ab8 |
|---|
| Source note | uspto-grants-2000_04 |
|---|