HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoic Acid → Benzoyl chloride, 2-butoxy-6-nitro-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoic Acid | HCID 243 | — |
| Reactant | Butyl iodide | HCID 10962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-Hydroxy-6-nitrobenzoic acid | HCID 14943903 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Benzoyl chloride, 2-butoxy-6-nitro- | HCID 19805532 | — |
Reaction Steps
Ra=4-butoxy, Rb=H. 2-Butoxy-6-nitrobenzoyl chloride was prepared by the reaction of thionyl chloride and the corresponding benzoic acid which, in turn, was prepared by hydrolysis of the corresponding butyl ester with sodium hydroxide in aqueous ethanol. The butyl ester was prepared by heating together a mixture containing 2-hydroxy-6-nitrobenzoic acid (Chem.Abs., 1963, 59, 500 g), butyl iodide, potassium carbonate and N,N-dimethylformamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05173496 |
| Source dataset | uspto-grants-1992_12 |
| ORD ID | ord-d9b757de6b7f473dae75346b1ca7aed6 |
| Source note | uspto-grants-1992_12 |