HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 5-(Aminosulphonyl)-2-methoxybenzoyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-Methoxy-5-sulfamoylbenzoic acid | HCID 89601 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-(Aminosulphonyl)-2-methoxybenzoyl chloride | HCID 104228 | — |
Reaction Steps
To a suspension of the so-obtained 2-methoxy-5-sulfamoyl benzoic acid in 600 parts of anhydrous tetrahydrofuran, there were added rapidly 27.5 parts of thionyl chloride. The mixture was refluxed for 2 hours. The solution was then evaporated under vacuo. The residue was treated with 500 parts of anhydrous benzene. After elimination of benzene in vacuo, there were obtained 29 parts of 2-methoxy-5-sulfamoyl benzoyl chloride, M.P. 148°-150° C., which after one recrystallization from benzene melts at 156° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04042598 |
| Source dataset | uspto-grants-1977_08 |
| ORD ID | ord-42493323a870418c8c540c0c2eda2885 |
| Source note | uspto-grants-1977_08 |