HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 5-(4-Aminophenyl)-2-Methyl-3-Furoate → Ethyl 5-(4-hydroxyphenyl)-2-methyl-3-furanecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 5-(4-Aminophenyl)-2-Methyl-3-Furoate | HCID 2742184 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | Ethyl 5-(4-hydroxyphenyl)-2-methyl-3-furanecarboxylate | HCID 22648859 | 20% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
A solution of NaNO2 (111 mg, 1.61 mmol) in water (1 mL) was added over 5 min to an ice-cold suspension of ethyl 5-(4-aminophenyl)-2-methyl-3-furanecarboxylate (395 mg, 1.61 mmol) in aqueous 1 M H2SO4 solution (12 mL). The reaction mixture was stirred at 0° C. for 20 min then was heated to 90° C. for 1 h. The cooled mixture was extracted with EtOAc. The organic layer was washed with water (2×) and brine, dried (MgSO4), filtered and concentrated under reduced pressure to yield the title compound (78 mg, 20% yield) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06806265B2 |
| Source dataset | uspto-grants-2004_10 |
| ORD ID | ord-371b50119d0c4c279cf533262f1fe6ab |
| Source note | uspto-grants-2004_10 |