HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 2-Methyl-4,5-di(methylsulfonyl)benzoyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-methyl-4,5-bis(methylsulfonyl)benzoic Acid | HCID 11266313 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Methyl-4,5-di(methylsulfonyl)benzoyl chloride | HCID 11088214 | — |
Reaction Steps
15 l of thionyl chloride are initially introduced at 40°, and 50 ml of DMF are added. 3.8 kg of 4,5-bismethanesulfonyl-2-methylbenzoic acid are slowly introduced with stirring, and the mixture is then stirred at the boiling point for 1 hour. After cooling, the excess SOCl2 is removed, and the residue is codistilled a number of times with 5 l of toluene, giving 4, 5-bismethanesulfonyl-2-methylbenzoyl chloride, which is reacted further as the crude product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06673968B1 |
| Source dataset | uspto-grants-2004_01 |
| ORD ID | ord-ee33cefa89264912ba9eb28eb36340f3 |
| Source note | uspto-grants-2004_01 |