HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzocaine → 4-{[2-(4-Fluorophenyl)ethyl]amino}benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzocaine | HCID 2337 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Hexamethylphosphoramide | HCID 12679 | — |
| Reactant | 1-(2-Chloroethyl)-4-fluorobenzene | HCID 67622 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-{[2-(4-Fluorophenyl)ethyl]amino}benzoic acid | HCID 13079680 | — |
Reaction Steps
A mixture of 15.8 g. of 1-(2-chloroethyl)-4-fluorobenzene, 33 g. of ethyl p-aminobenzoate, 16.6 g. of potassium iodide and 100 ml. of hexamethylphosphoramide is heated at 95° C. for 15 hours. The mixture is poured into water and extracted with ether. The ether extracts are washed with water, dried over magnesium sulfate and concentrated in vacuo to an oil. To the oil is added 200 ml. of ethanol-water (9:1) and 21 g. of potassium hydroxide and the mixture is refluxed for 3.5 hours. The mixture is acidified with concentrated hydrochloric acid, diluted with water, cooled and filtered to give gray crystals. Recrystallization from ethanol gives light gray crystals, m.p. 161°-163° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04185115 |
| Source dataset | uspto-grants-1980_01 |
| ORD ID | ord-85bae272d5f54f1ea7d908f75b33abad |
| Source note | uspto-grants-1980_01 |