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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2039413Generated: October 29, 2026

Iodine → 4-Bromo-2-iodo-1-methylbenzene

https://huagongshe.com/reaction/2039413

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSulfuric AcidHCID 1118—
Reactant4-BromotolueneHCID 7805—
ReactantSodium periodateHCID 23667635—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventAcetic AnhydrideHCID 7918—
Product4-Bromo-2-iodo-1-methylbenzeneHCID 15442947197.9%

Reaction Conditions

Temperature10 °C

Reaction Steps

Sodium periodate (0.5 molar equivalent, 102.5 g, 0.48 mol) and iodine (0.3 molar equivalent, 81.6 g, 0.32 mol) are suspended in acetic acid (700 ml) and acetic anhydride (340 ml). The batch is then cooled to 10° C., and sulfuric acid (2.9 molar equivalents, 142 ml, 2.66 mol) is slowly added dropwise at this temperature. 4-Bromotoluene 5 (1 molar equivalent, 160.7 g, 0.94 mol) is subsequently slowly added dropwise at room temperature, and the batch is stirred overnight. After addition of cooled water (1000 ml) and a solution of Na2SO3 (169 g in 1000 ml), the mixture is extracted by shaking with dichloromethane (DCM). The organic phase is washed with water, dried and evaporated in a rotary evaporator. The product 6 (188.0 g, 67%) is obtained in the form of a liquid by vacuum distillation.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580395B2
Source datasetuspto-grants-2013_11
ORD IDord-a29068e99bac4ee09e9a0fe49fd3508e
Source noteuspto-grants-2013_11