HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 2-Bromo-3-methyl-5-nitrobenzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl 2-bromo-3-methyl-5-nitrobenzoate | HCID 23433653 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Bromo-3-methyl-5-nitrobenzoic acid | HCID 21469187 | 94.1% |
Reaction Steps
To a solution of 2-bromo-3-methyl-5-nitro-benzoic acid methyl ester ((Example 295: step d) 5.04 g) in ethanol (50 mL) was added a solution of aq NaOH (4M, 1.62 g, 40.5 mmol) and stirred at ambient temperature for 16 h. The resulting red colored solution was concentrated to dryness, dissolved in a minimum amount of H2O, and acidified with 1 N HCl to pH 3–4. The solid was filtered, washed with H2O (3×50 mL) dried under high vacuum to afford the title compound (4.5 g, 94% yield) as a pale yellow solid. 1H NMR (DMSO) δ 8.36–8.35 (m, 1H), 8.24–8.23 (m, 1H), 2.53 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07138530B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-47f099dd446d41c88dabd5c7b34f457a |
| Source note | uspto-grants-2006_11 |