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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
ReactantN-bromobutanimideHCID 67184—
ReactantMethyl 5-methyl-2-nitrobenzoateHCID 3314122—
CatalystAzobisisobutyronitrileHCID 6547—
SolventCarbon TetrachlorideHCID 5943—
SolventSodium chloride; waterHCID 57417360—
ProductMethyl 5-azidomethyl-2-nitrobenzoateHCID 1969836456%

Reaction Conditions

Temperature50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05719152
Source datasetuspto-grants-1998_02
ORD IDord-7c698477cf64466a9842f66780c05685
Source noteuspto-grants-1998_02