HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl 2-methyl-6-nitrobenzoate → Allyl 2-amino-6-methylbenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl 2-methyl-6-nitrobenzoate | HCID 19432516 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Allyl 2-amino-6-methylbenzoate | HCID 19432484 | 75% |
Reaction Steps
Stannous chloride dihydrate (15.3 g, 67.8 mM) was suspended in methanol (25 ml), and a solution of allyl 2-methyl-6-nitrobenzoate (3.0 g, 13.6 mM) in methanol (5 ml) was added. The mixture was heated at reflux for 1 hour, cooled, and solvent removed. The residue was treated with ethyl acetate (100 ml), made basic with 880 ammonia and diluted with water (50 ml). The organic layer was decanted from the slurry of tin salts, which was extracted with two further portions of ethyl acetate. The combined organic extracts were washed with dilute ammonia, water, brine, and dried over MgSO4, to give allyl 2-amino-6-methylbenzoate as an oil (1.94 g, 75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05541178 |
| Source dataset | uspto-grants-1996_07 |
| ORD ID | ord-a6a9c3170fca4416b242b4f60ca75e49 |
| Source note | uspto-grants-1996_07 |