HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 3,5-Dinitrobenzoyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 3,5-Dinitrobenzoic acid | HCID 7433 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2,3-Dinitrobenzoic acid | HCID 283327 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3,5-Dinitrobenzoyl chloride | HCID 7432 | 90% |
Reaction Steps
3,5 dinitrobenzoic acid and ethyl acetate were placed in a reaction vessel. While thionyl chloride with some drops of DMF (about double as many moles as dinitrobenzoic acid) was dropped into the reaction mixtures, the reaction mixtures were refluxed with stirring until the generation of hydrogen chloride gas stopped. The reacted solution was concentrated until a solid could be precipitated and was poured into hexane and then the precipitated solid was separated by filtration. 3,5-dinitrobenzoic chloride was obtained in a 90% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06689899B2 |
| Source dataset | uspto-grants-2004_02 |
| ORD ID | ord-d9c86f8ebb574201a1828d0d9adf8e43 |
| Source note | uspto-grants-2004_02 |