HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 862568Generated: October 31, 2026
Sodium Azide → Methyl 5-azidomethyl-2-nitrobenzoate
https://huagongshe.com/reaction/862568
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Methyl 5-methyl-2-nitrobenzoate | HCID 3314122 | — |
| Catalyst | Azobisisobutyronitrile | HCID 6547 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | Methyl 5-azidomethyl-2-nitrobenzoate | HCID 19698364 | 56% |
Reaction Steps
A mixture of methyl 5-methyl-2-nitrobenzoate (5.5 g, 30 mmol), N-bromosuccinimide (NBS, 5.87 g, 33 mmol), and azobisisobutyronitrile (AlBN, 200 mg) in carbon tetrachloride (60 mL) was refluxed for 3 h. The insoluble material formed was removed by filtration and the filtrate was concentrated. The residue was dissolved in DMF (10 mL) and sodium azide (2.92 g, 45 mmol) was added. The mixture was stirred for 2 h at 50° C., poured into brine, and extracted with a 1:1 mixture of toluene and ethyl acetate. The organic layers were washed with brine, dried over magnesium sulfate, and concentrated. The residue was purified by silica gel column chromatography with 4:1 hexane/ethyl acetate to give 3.97 g of the title compound (56%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05719152 |
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| Source dataset | uspto-grants-1998_02 |
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| ORD ID | ord-7c698477cf64466a9842f66780c05685 |
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| Source note | uspto-grants-1998_02 |
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