HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoic acid, 4-hydroxy-3-nitro-, methyl ester → Methyl 3-bromo-4-hydroxy-5-nitrobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoic acid, 4-hydroxy-3-nitro-, methyl ester | HCID 66835 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Methyl 3-bromo-4-hydroxy-5-nitrobenzoate | HCID 14985559 | 95.3% |
Reaction Steps
(I4A): Methyl 4-hydroxy-3-nitrobenzoate (15 g, 76 mmol) was suspended in acetic acid (152 ml) and then treated with NBS (20.31 g, 114 mmol). The mixture became a homogeneous yellow solution which was stirred for 2 h. The mixture was quenched with water and the suspension was filtered. Methyl 3-bromo-4-hydroxy-5-nitrobenzoate (20 g) was obtained as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09273057B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-0d65dac8ba0e44089f74eec7e92252da |
| Source note | uspto-grants-2016_03 |