HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1022482Generated: November 1, 2026
Ammonium Chloride → Ethyl 2-amino-5-(benzyloxy)-4-fluorobenzoate
https://huagongshe.com/reaction/1022482
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Ethyl 5-(benzyloxy)-4-fluoro-2-nitrobenzoate | HCID 67495361 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 2-amino-5-(benzyloxy)-4-fluorobenzoate | HCID 61994641 | 82% |
Reaction Steps
1.76 g of NH4Cl dissolved in 21 ml of water are added to a mixture heated to 90° C. of 7.0 g of the compound obtained in Step 4.1, and 4.44 g of Fe(0) in 400 ml of isopropanol and 100 ml of THF. The reaction mixture is heated for 4 hours at 90° C. A further 0.88 g of NH4Cl is added and the mixture is heated for 2 hours at 90° C. The resulting mixture is filtered while hot and the filtrate is evaporated under reduced pressure. The residue is taken up in EtOAc and washed twice with saturated NaHCO3 solution. The organic phase is dried over MgSO4 and filtered, and the filtrate is evaporated under reduced pressure. The residue is chromatographed on silica gel, eluting with a PE/EtOAc mixture from (100/0, v/v) to (40/60, v/v) to give 5.2 g of the expected product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08722659B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-9376898b46c241288c347f0fe15abec6 |
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| Source note | uspto-grants-2014_05 |
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