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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1288713Generated: October 27, 2026

Potassium Iodide → Methyl 3-iodo-2-methyl-6-(1-methylethylsulphenyl)benzoate

https://huagongshe.com/reaction/1288713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium NitriteHCID 23668193—
ReactantMethyl 3-amino-2-methyl-6-(1-methylethylsulphenyl)-benzoateHCID 54177219—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
ProductMethyl 3-iodo-2-methyl-6-(1-methylethylsulphenyl)benzoateHCID 5389199977.8%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of sodium nitrite (6.7 g) in water was added to a stirred, cooled mixture of methyl 3-amino-2-methyl-6-(1-methylethylsulphenyl)-benzoate (18 g) in concentrated hydrochloric acid while maintaining the temperature below 0° C. The resultant mixture was added to a solution of potassium iodide (16 g) in water while maintaining the temperature at about 80° C. The resultant mixture was stirred at 80° C. for 15 mins then cooled to room temperature. It was diluted with water and extracted with dichloromethane. The organic layer was washed with sodium bicarbonate solution, water, dried (MgSO4) and filtered. The filtrate was evaporated to dryness to give methyl 3-iodo-2-methyl-6-(1-methylethylsulphenyl)benzoate (20.5 g) as a red oil. NMR (CDCl3) 1.25 (d,6H) 2.35(s,3H) 3.2(m,1H) 3.9(s,3H) 6.9(d,1H) 7.6(d, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05747424
Source datasetuspto-grants-1998_05
ORD IDord-aeaf38b1d20d45369819f16b023d739b
Source noteuspto-grants-1998_05