HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 631373Generated: October 25, 2026
Potassium Iodide → Methyl 5-Benzyloxy-4-methoxy-2-nitrobenzoate
https://huagongshe.com/reaction/631373
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 5-hydroxy-4-methoxy-2-nitrobenzoate | HCID 53396387 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 5-Benzyloxy-4-methoxy-2-nitrobenzoate | HCID 22667156 | 77.1% |
Reaction Steps
To solution of methyl 5-hydroxy-4-methoxy-2-nitrobenzoate (13.0 g, 0.0572 mol) in DMF (120 mL) and benzyl chloride (7.23 ml, 0.0629 mol), K2CO3 (8.69 g, 0.0629 mol) and potassium iodide (0.949 g, 0.0057 mol) were added. The reaction mixture was heated at 90-95° C. overnight. The solvent was evaporated under vacuum and the residue was taken in ethyl acetate and washed with water and brine. After drying over MgSO4, the solution was concentrated ad purified on silica gel column to yield methyl 5-(benzyloxy)-4-methoxy-2-nitrobenzoate (13.99 g, 77% yield). 1HNMR (DMSO-d6): δ 7.66 (1H, s), 7.40 (6H, m), 5.27 (2H, s), 3.83 (3H, s), 3.80 (3H, s). LC-MS (ESI) m/z 318 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09320739B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-006e04c5f87743a5919f4eeaec6a8f5b |
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| Source note | uspto-grants-2016_04 |
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