HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 2-methyl-7-nitro-2,3-dihydrobenzofuran-4-carboxylate → Methyl 7-amino-2-methyl-2,3-dihydrobenzofuran-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 2-methyl-7-nitro-2,3-dihydrobenzofuran-4-carboxylate | HCID 68107419 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 7-amino-2-methyl-2,3-dihydrobenzofuran-4-carboxylate | HCID 68107846 | 91.9% |
Reaction Steps
Methyl 2-methyl-7-nitro-2,3-dihydrobenzofuran-4-carboxylate 30a (100 mg, 0.42 mmol) was dissolved in 20 mL of methanol followed by the addition of palladium/carbon (10 mg, 10%), filled with hydrogen for three times. The reaction solution was stirred for 12 hours and filtered. The filtrate was concentrated under reduced pressure to obtain the title compound methyl 7-amino-2-methyl-2,3-dihydrobenzofuran-4-carboxylate 30b (80 mg, yield: 91.0%) as a colorless oil liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08691822B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-650d439649754ea690b74b723fcf9474 |
| Source note | uspto-grants-2014_04 |