HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 3-methyl-4-(2-methoxy-5-nitrophenoxy)butyrate → Methyl 3-methyl-4-(2-methoxy-5-aminophenoxy)butyrate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 3-methyl-4-(2-methoxy-5-nitrophenoxy)butyrate | HCID 18433387 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 3-methyl-4-(2-methoxy-5-aminophenoxy)butyrate | HCID 11322746 | — |
Reaction Steps
At ambient temperature a rapidly stirred solution of methyl 3-methyl-4-(2-methoxy-5-nitrophenoxy)butyrate(400 mg) in methanol (20 mL) containing 10% palladium on carbon (40 mg) was exposed to an atmosphere of hydrogen. When uptake of hydrogen had ceased the solution was filtered and the filter cake washed with methanol. The combined filtrates were evaporated to dryness under reduced pressure, to give methyl 3-methyl-4-(2-methoxy-5-aminophenoxy)butyrate as an oil. (317 mg) m/Z 254(M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06441012B1 |
| Source dataset | uspto-grants-2002_08 |
| ORD ID | ord-3f77f4683d644ee1a3028b3cc4762386 |
| Source note | uspto-grants-2002_08 |