HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193484Generated: October 25, 2026
Benzyl Bromide → 1-Benzyloxy-3-methyl-2-nitrobenzene
https://huagongshe.com/reaction/1193484
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Methyl-2-nitrophenol | HCID 21026 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-Benzyloxy-3-methyl-2-nitrobenzene | HCID 3344187 | 88.3% |
Reaction Steps
A mixture of 3-methyl-2-nitrophenol (50 g, 0.326 mol), K2CO3 (45 g, 0.326 mol) and benzylbromide (61.4 g, 42.6 mL, 0.359 mol) in dry DMF (200 mL) was stirred at 90° C. for 3 hours under nitrogen. Most of the DMF was removed at reduced pressure and the residue was partitioned between water (300 mL) and ether (300 mL). The organic layer was washed with brine and dried (Na2SO4). Removal of the solvent provided (70 g, 88%) of 3-benzyloxy-2-nitrotoluene as an orange oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04810699 |
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| Source dataset | uspto-grants-1989_03 |
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| ORD ID | ord-a704537da871413fb26b32dab55ba06d |
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| Source note | uspto-grants-1989_03 |
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