HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Chloro-2-methyl-6-nitro-1,3-benzoxazole → 2-Methyl-5-chloro-6-benzoxazolamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Chloro-2-methyl-6-nitro-1,3-benzoxazole | HCID 2764455 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Methyl-5-chloro-6-benzoxazolamine | HCID 11275404 | — |
Reaction Steps
Compound (2), (30 g), was dissolved in tetrahydrofuran (150 mL), and Raney-Nickel which had been pre-washed with water (×3) and tetrahydrofuran (×3), was added. The mixture was then hydrogenated at room temperature and 50 psi of hydrogen. The reaction is complete in approximately 1.5 hours. After this period, the catalyst is filtered off and the solution concentrated under reduced pressure. The residue is triturated with heptane, cooled and the solid filtered off. Yield 22 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06194132B1 |
| Source dataset | uspto-grants-2001_02 |
| ORD ID | ord-26f2160b0298461eb5623b55f0d3e78b |
| Source note | uspto-grants-2001_02 |