HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 497058Generated: October 26, 2026
Hydrochloric Acid → Ethyl {4-[benzyloxycarbonylmethyl-(4-fluorobenzoyl)amino]phenoxy)acetate
https://huagongshe.com/reaction/497058
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Benzyl bromoacetate | HCID 62576 | — |
| Reactant | 4-Fluorobenzoyl chloride | HCID 67879 | — |
| Reactant | Ethyl 2-(4-aminophenoxy)acetate | HCID 412616 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl {4-[benzyloxycarbonylmethyl-(4-fluorobenzoyl)amino]phenoxy)acetate | HCID 91495284 | — |
Reaction Steps
Potassium carbonate and benzyl bromoacetate were added to DMF solution of ethyl (4-aminophenoxy)acetate and stirred under heating. After adding water and ethyl acetate to the reaction mixture, the organic layer was separated, washed and dried, and then the solvent was evaporated under a reduced pressure. Dichloromethane solution of the thus obtained crude product was mixed with TEA, 4-fluorobenzoyl chloride was added dropwise thereto under ice-cooling and then the reaction solution was stirred. After adding 1 M hydrochloric acid to the reaction solution, the organic layer was separated, washed and dried, and then the solvent was evaporated under a reduced pressure. By purifying the thus obtained crude product by SCG, ethyl {4-[benzyloxycarbonylmethyl-(4-fluorobenzoyl)amino]phenoxy}acetate (colorless oil) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06949543B2 |
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| Source dataset | uspto-grants-2005_09 |
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| ORD ID | ord-fc898232bff74f0d91c4f86377031b66 |
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| Source note | uspto-grants-2005_09 |
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