HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004871Generated: October 25, 2026
Oxalyl chloride → 2-Chlorobenzoyl isocyanate
https://huagongshe.com/reaction/1004871
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 2-Chlorobenzamide | HCID 69111 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 2-Chlorobenzoyl isocyanate | HCID 9942311 | — |
Reaction Steps
0.42 g (2.7 mmol) of 2-chlorobenzamide 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-chlorobenzoyl 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 1.0 g (Yield 84%) of the title compound as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06051737 |
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| Source dataset | uspto-grants-2000_04 |
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| ORD ID | ord-8bb7848e35aa40d5afa00537acbffed2 |
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| Source note | uspto-grants-2000_04 |
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