HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-Chloroacetylamino-5-ethoxycarbonyl-4,6-dimethylbenzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | 2-Amino-5-ethoxycarbonyl-4,6-dimethylbenzoic acid | HCID 12685840 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-Chloroacetylamino-5-ethoxycarbonyl-4,6-dimethylbenzoic acid | HCID 12912436 | — |
Reaction Steps
To an ice-cooled mixture consisting of 0.8 g of 2-amino-5-ethoxycarbonyl-4,6-dimethylbenzoic acid, 20 ml of dry benzene, and 0.5 ml of pyridine was added dropwise with stirring a solution of 0.4 ml of chloroacetyl chloride in 5 ml of benzene. The mixture was stirred overnight and then, shaken with dilute hydrochloric acid. The layers were separated. The aqueous layer was extracted with ethyl acetate, and the combined organic extracts were washed with water, dried over sodium sulfate, and evaporated. The residue was recrystallized from ethyl ether/n-hexane to give 0.65 g of 2-chloroacetylamino-5-ethoxycarbonyl-4,6-dimethylbenzoic acid (m.p. 124°-125° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04276295 |
| Source dataset | uspto-grants-1981_06 |
| ORD ID | ord-ed721349c55e4a99ada2ecf3e4faa220 |
| Source note | uspto-grants-1981_06 |