HuagongsheHuagongshe Chemistry Print Report · For research reference only
Stannous chloride dihydrate → Methyl 3-amino-6-chloro-2-methylbenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Stannous chloride dihydrate | HCID 61436 | — |
| Reactant | HCID 68749648 | HCID 68749648 | — |
| Reactant | HCID 68754758 | HCID 68754758 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Methyl 3-amino-6-chloro-2-methylbenzoate | HCID 21710154 | — |
Reaction Steps
To above stirred mixture of methyl 6-chloro-2-methyl-3-nitrobenzoate 62 and methyl 6-chloro-2-methyl-5-nitrobenzoate in EtOH (500 mL), SnCl2.2H2O (224 g, 992 mmol, 4 eq) was added and the resulting mixture was stirred at reflux for 3 h. The reaction mixture was allowed to cool to RT and concentrated in vacuo. The residue was poured into water (1 L) and extracted with ethyl acetate (5×500 mL). The combined organic layers were washed with brine, dried over Na2SO4 and filtered. The filtrate was concentrated in vacuo and the residue was purified by flash column chromatography on silica gel (2-10% ethyl acetate-hexanes) to afford the regio-isomer methyl 3-amino-6-chloro-2-methylbenzoate 63.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09388183B2 |
| Source dataset | uspto-grants-2016_07 |
| ORD ID | ord-af7400a89cea4894a38fcf4454f20405 |
| Source note | uspto-grants-2016_07 |