Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2089267Generated: October 31, 2026

Nitric Acid → 4-Iodo-3-nitrothioanisole

https://huagongshe.com/reaction/2089267

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantDimethyl SulfateHCID 6497—
Reactant1-Iodo-4-(methylsulfanyl)benzeneHCID 2759374—
SolventSulfuric AcidHCID 1118—
Product4-Iodo-3-nitrothioanisoleHCID 5975458080%

Reaction Conditions

Temperature90 °C

Reaction Steps

A flask was charged with 10 g of 4-iodothioanisole and 5.5 mL of dimethylsulfate and warmed to ca. 90° C. for 10 min. The resulting solution was dissolved in conc. sulfuric acid (30 mL) and cooled to ca. 0-4° C., whereupon it was treated, with extreme caution, slowly with conc. HNO3 (ca. 2 mL) while maintaining the reaction temperature below 4° C. After stirring it for ca. 10 min, the reaction mixture was stirred at ca. 90° C. for ca. 3 d. The reaction was monitored with HPLC, TLC, and LC-MS, and if needed, smaller portions of nitric acid were added to the reaction mixture to force it to completion. Use of fuming sulfuric acid is also helpful. After the complete consumption of the aromatic starting material, the reaction mixture was cooled, poured over crushed ice, treated with 30% aq. perchloric acid at 4° C. The light colored precipitate was filtered, washed thoroughly with water, and dried under vacuum. The perchlorate salt was stirred with saturated aq. NaCl solution at 95° C. for 3-6 h. Upon cooling to room temperature, the precipitate was filtered, washed thoroughly with water to get rid of any inorganic salts, and dried under vacuum to obtain 4-iodo-3-nitrothioanisole in >80% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436031B2
Source datasetuspto-grants-2013_05
ORD IDord-122290786c8149acbb0e9815bd9073bc
Source noteuspto-grants-2013_05