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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2421538Generated: November 2, 2026

Sodium Iodide → 1,3-Dibromo-2-iodo-5-nitrobenzene

https://huagongshe.com/reaction/2421538

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantDimethylformamideHCID 6228—
Reactant2,6-Dibromo-4-nitrophenyl triflateHCID 10202874—
SolventWaterHCID 962—
Product1,3-Dibromo-2-iodo-5-nitrobenzeneHCID 1015827982.9%

Reaction Conditions

Temperature100 °C

Reaction Steps

Dimethylformamide (4 L) and trifluoromethane sulfonic acid 2,6-dibromo-4-nitrophenyl ester (1135 g, 2.65 moles) were charged into a 22 L jacketed vessel equipped with a mechanical stirrer, a condenser, and a nitrogen purge. Sodium iodide (1595 g, 10.64 moles) was added to the reaction mixture in portions while maintaining the reaction temperature below 25° C. The reaction mixture was then heated to 100° C. and monitored for completion by HPLC. Upon completion, the reaction mixture was cooled to 0° C. Water (4 L) was added while maintaining the temperature below 14° C. The reaction mixture was stirred for 30 min, then filtered and washed with water (1.5 L). The resultant solid product was dried overnight by evaporation under air flow at room temperature to yield 1,3-dibromo-2-iodo-5-nitrobenzene (892.7 g, 82.9%). The product may optionally be purified further by recrystallization from ethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07956214B2
Source datasetuspto-grants-2011_06
ORD IDord-f287b6a707d94ce9ba1acb4038f362d3
Source noteuspto-grants-2011_06