HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384295Generated: October 30, 2026
Ammonium formate → 3'-Amino-5'-fluoro-2'-hydroxy-biphenyl-3-carboxylic acid
https://huagongshe.com/reaction/384295
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | 3'-Nitro-5'-fluoro-2'-hydroxy-biphenyl-3-carboxylic acid hydrobromide | HCID 68673169 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3'-Amino-5'-fluoro-2'-hydroxy-biphenyl-3-carboxylic acid | HCID 21072315 | 91.5% |
Reaction Steps
3′-Nitro-5′-fluoro-2′-hydroxy-biphenyl-3-carboxylic acid hydrobromide 2e (417 mg, 1.5 mmol) was dissolved in 60 mL of ethanol followed by addition of 0.5 g of palladium on carbon and ammonium formate (0.95 g, 1.5 mmol). The reaction mixture was heated to reflux at 80° C. for 20 minutes. The reaction was monitored by TLC until the disappearance of the starting materials. The mixture was filtered and the filtrate was concentrated under reduced pressure and dried to obtain the title compound 3′-amino-5′-fluoro-2′-hydroxy-biphenyl-3-carboxylic acid 2f (339 mg, yield 91.5%) as a purple solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08367710B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-cb83fc022dd14e93ae63ccda1bd5d79f |
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| Source note | uspto-grants-2013_02 |
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