HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → 5-Chloroisatoic anhydride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 2-[(tert-Butoxycarbonyl)amino]-6-chlorobenzoic acid | HCID 17750447 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-Chloroisatoic anhydride | HCID 78480 | — |
Reaction Steps
After suspending 2-(Boc)amino-6-chlorobenzoic acid (1.51 g, 5.56 mmol) in toluene (20 mL), the mixture was heated to reflux. Oxalyl chloride (0.572 mL, 6.67 mmol) was added dropwise thereto, and the mixture was vigorously stirred for 10 minutes. After cooling the reaction mixture on ice, the precipitated crystals were filtered out, washed with n-hexane and dried in a desiccator to obtain 5-chloroisatoic anhydride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07517875B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-f70b25d3c94f4b0ea9b6af9c6d3fc4b9 |
| Source note | uspto-grants-2009_04 |