Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18670Generated: October 27, 2026

Hydrochloric Acid → 5-Iodo-2-isopropyl-4-methoxyphenol

https://huagongshe.com/reaction/18670

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHexaneHCID 8058—
ReactantPotassium HydroxideHCID 14797—
Reactant5-Iodo-4-methoxy-2-(propan-2-yl)phenyl 4-methylbenzene-1-sulfonateHCID 44248853—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
Product5-Iodo-2-isopropyl-4-methoxyphenolHCID 4424885484%

Reaction Steps

To a mixture of 292 grams of toluene-4-sulfonic acid 5-iodo-2-isopropyl-4-methoxy-phenyl ester (0.66 Moles) in 600 mL tert-butyl alcohol was gradually added a solution of 90 g KOH in 400 mL water, and the resultant mixture was stirred overnight at 82 degrees C. The reaction mixture was neutralized with conc. HCl to a pH of 5-6, and then partitioned between 600 mL ethyl acetate and 400 mL water. The organic phase was dried over sodium sulfate, filtered and stripped under vacuum at 65 degrees C. to give a resinous liquid. Hexane (700 mL) was then added and the mixture heated to reflux. The liquid phase was decanted into another flask and stirred overnight at room temperature, during which time a white solid precipitated. The solid was isolated by filtration and vacuum dried to give 162 g of 5-iodo-2-isopropyl-4-methoxy-phenol, representing a yield of 82%: MS (M+H)=293.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741484B2
Source datasetuspto-grants-2010_06
ORD IDord-bbaaf7add8944043a4edf897e71c23fc
Source noteuspto-grants-2010_06