HuagongsheHuagongshe Chemistry Print Report · For research reference only
Stannous Chloride → Methyl 5-amino-4'-methylbiphenyl-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Stannous Chloride | HCID 24479 | — |
| Reactant | Methyl 3-(4-methylphenyl)-5-nitrobenzoate | HCID 57851213 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 5-amino-4'-methylbiphenyl-3-carboxylate | HCID 57850917 | 95.2% |
Reaction Steps
To a solution of 4′-Methyl-5-nitro-biphenyl-3-carboxylic acid methyl ester (10.00 g, 36.9 mmol) in methanol was added SnCl2 (27.98 g, 147.6 mmol) at room temperature. The reaction mixture was refluxed for 3 hours, then cooled. Solvent was removed in vacuo and the residue was dissolved in H2O, then basified by addition of Na2CO3 to pH=9. The mixture was extracted by CH2Cl2, and the organic phase was washed with water followed by brine, and dried over Na2SO4. The solvent was removed under vacuum to give 5-Amino-4′-methyl-biphenyl-3-carboxylic acid methyl ester (8.48 g, 95%) as yellow oil. MS (M+H)=242.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08193368B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-339015546fbc4a8a90eb4f7f9029da0e |
| Source note | uspto-grants-2012_06 |