HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → 3-(Chlorosulfonyl)-4-fluorobenzoyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 3-(Chlorosulfonyl)-4-fluorobenzoic acid | HCID 3929891 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(Chlorosulfonyl)-4-fluorobenzoyl chloride | HCID 58107439 | — |
Reaction Steps
To a suspension of 3-chlorosulfonyl-4-fluoro benzoic acid (2.5 g, 10 mmol) in methylene chloride at 0° C. is added oxalyl chloride (1.33 g, 11 mmol), followed by the addition of 1 drop of N,N,-dimethylformamide. The reaction mixture is warmed up to room temperature and stirred for an additional 4 h. The solvent is removed, and the residue is dried under vacuum for 1 hr to obtain the title compound as an oil, which is used for the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08362063B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-81214e6fffcc478c925030ad5c2c7af3 |
| Source note | uspto-grants-2013_01 |