HuagongsheHuagongshe Chemistry Print Report · For research reference only
Salicylic Acid → HCID 54207586, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Salicylic Acid | HCID 338 | — |
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Reactant | 2,5-Dichlorobenzooxazole | HCID 10397578 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 54207586 | HCID 54207586 | — |
Reaction Steps
Substantially equimolar amounts of 2,5-dichlorobenzoxazole and the potassium salt of 2-hydroxy benzoic acid are reacted, in an inert organic solvent, e.g., dimethylsulfoxide, in the presence of acetic acid giving 5-(5-chloro-2-benzoxazolyloxy) benzoic acid. The benzoate is then nitrated by, for example, reaction with a mixture of nitric acid, sulfuric acid and acetic anhydride to give the corresponding 2-nitrobenzoic acid prepared as previously described. The 2-nitrobenzoic acid is then reacted with ethyl 2-chloropropionate, as previously described, giving the desired 1-(ethoxycarbonyl)ethyl 5-(5-chloro-2-benzoxazolyloxy)-2-nitrobenzoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04468244 |
| Source dataset | uspto-grants-1984_08 |
| ORD ID | ord-383d6e1b37564f7bb4a895cfc86eb016 |
| Source note | uspto-grants-1984_08 |