HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355809Generated: October 28, 2026
Benzocaine → Ethyl 4-[2-benzyloxy-5-bromophenylacetamido]benzoate
https://huagongshe.com/reaction/355809
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzocaine | HCID 2337 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-[2-(Benzyloxy)-5-bromophenyl]acetic acid | HCID 3307011 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 4-[2-benzyloxy-5-bromophenylacetamido]benzoate | HCID 54475189 | 42.9% |
Reaction Steps
To a mixture of 2-benzyloxy-5-bromophenylacetic acid (3.2 g) in toluene (100 ml) was added thionyl chloride (1.0 ml) and DMF (3 drops ). The reaction was stirred at 80° C. for 1 hour and cooled to ambient temperature. ethyl 4-aminobenzoate (2.0 g) and triethylamine (2 ml) were added to the reaction mixture with stirring. After standing for 18 hours, the mixture was diluted with dichloromethane and washed with water, 1N HCl solution, water and sautrated aqueous NaHCO3 solution. The organic extract was dried (MgSO4), filtered and evaporated and the residue purified by trituration with diethyl ether to give ethyl 4-[2-benzyloxy-5-bromophenylacetamido]benzoate (2.0 g) mpt. 174°-176° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05834468 |
|---|
| Source dataset | uspto-grants-1998_11 |
|---|
| ORD ID | ord-99db7a75acb44c3f8d1d80065c95b309 |
|---|
| Source note | uspto-grants-1998_11 |
|---|