HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-Fluoro-3-hydroxy-4-nitrophenylacetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 67406367 | HCID 67406367 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-Fluoro-3-hydroxy-4-nitrophenylacetic acid | HCID 58778490 | — |
Reaction Steps
Di-tert-butyl (3-benzyloxy-2-fluoro-4-nitrophenyl)malonate (6.87 g, 14.9 mmol), acetic acid (200 ml) and concentrated hydrochloric acid (35 ml) were stirred at 120° C. for 6 hours. After cooling to room temperature, the reaction mixture was concentrated under reduced pressure, whereby the title compound was obtained as a brown oil (this compound was provided for the subsequent reaction without further purification).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07157487B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-440e16a1e17a46c7ac22f6000529ba7c |
| Source note | uspto-grants-2007_01 |