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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1065557Generated: October 26, 2026

Sulfuric Acid → (3-Iodo-2-methylphenyl)methanol

https://huagongshe.com/reaction/1065557

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantPotassium IodideHCID 4875—
Reactant(3-Amino-2-methylphenyl)methanol hydrochlorideHCID 20270659—
ReactantSodium NitriteHCID 23668193—
CatalystCopperHCID 23978—
SolventWaterHCID 962—
Product(3-Iodo-2-methylphenyl)methanolHCID 1503550624.5%

Reaction Steps

A stirred solution of 3-hydroxymethyl-2-methylaniline hydrochloride (43.4 g, 0.25 mole) and 17.2 ml of concentrated sulfuric acid in ice-water was cooled to 0°, and a solution of sodium nitrite (17.3 g, 0.25 mole) in water was added dropwise. Upon complete addition, the reaction mixture was stirred for an additional 0.5 hour, then an additional 8 ml of concentrated sulfuric acid was added dropwise. With the temperature maintained at 0°, a solution of potassium iodide (49.8 g, 0.30 mole) in water was added dropwise to the reaction mixture, followed by the addition of 0.1 gram of copper powder. The reaction mixture was slowly warmed to 70° where it stirred for 1 hour. The reaction mixture was then allowed to stand for 18 hours while cooling to room temperature. The reaction mixture was then taken up in water and extracted with chloroform. The chloroform extract was washed with an aqueous saturated solution of sodium bisulfite, then with water. The chloroform layer was dried and filtered. The filtrate was evaporated under reduced pressure to give 3-iodo-2-methylbenzyl alcohol (15.2 g) as a dark solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04329518
Source datasetuspto-grants-1982_05
ORD IDord-2de92ff7207b404abd0ed05b07f800d7
Source noteuspto-grants-1982_05