HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 928542Generated: October 30, 2026
Dimethylformamide → Methyl 3-(benzyloxy)-4-bromo-2-nitrobenzoate
https://huagongshe.com/reaction/928542
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 4-bromo-3-hydroxy-2-nitrobenzoate | HCID 58497911 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 3-(benzyloxy)-4-bromo-2-nitrobenzoate | HCID 21771685 | 97.4% |
Reaction Steps
A solution of methyl 4-bromo-3-hydroxy-2-nitrobenzoate (5.41 g, 19.6 mmol) and potassium carbonate (5.42 g, 39.2 mmol) in N,N-dimethylformamide (30 mL, 387 mmol) was treated with benzyl bromide (3.26 mL, 27.4 mmol) and stirred at 60° C. for 1 h. The reaction mixture was diluted with water (250 mL) and extracted with ethyl acetate (2×150 mL). The combined organic extracts were washed with brine, dried over sodium sulfate, filtered, and concentrated to give a crude tan oil. Purification by flash column chromatography (100% hexanes to 50% EtOAc/hexanes) gave the desired product (6.99 g, 97%) as a yellow solid. LCMS calculated for C15H16BrN2O5 (M+NH4)+: m/z=383.0, 385.0. found: 383.0, 385.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09290514B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-2c0ecb4e5543412c93c153abad1936c2 |
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| Source note | uspto-grants-2016_03 |
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