Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1602789Generated: November 1, 2026

Sulfuric Acid → 4-Iodo 2-methoxy biphenyl

https://huagongshe.com/reaction/1602789

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantPotassium IodideHCID 4875—
Reactant2-Methoxy-[1,1'-biphenyl]-4-amineHCID 521773—
ReactantSodium NitriteHCID 23668193—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product4-Iodo 2-methoxy biphenylHCID 1853348877.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

8 g of the product obtained in Stage B is dissolved at 40° C. in 60 ml of glacial acetic acid. Then a solution of 5 ml of concentrated sulphuric acid in 80 ml of water is added. The reaction medium is cooled down to 0° C. Then a solution of 2.77 g of sodium nitrite in 35 ml of water is added dropwise over one hour. Agitation is carried out for one hour at 0° C., and a solution of 13.33 g of potassium iodide, in 25 ml of water is added dropwise. The suspension obtained is maintained at 0° C. for one hour, brought to 10° C. over 40 minutes, maintained at 10° C. for one hour, and brought to 20° C. over 30 minutes. It is poured into water, and extraction is carried out with ethyl acetate. The organic phases are collected and washed (aqueous solution of NaHSO3 then NaHCO3). They are dried and evaporated under reduced pressure. The product obtained is chromatographed, eluting with a heptane-methylene chloride mixture (9-1) and 9.6 g of sought product is obtained, melting at 57° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05985853
Source datasetuspto-grants-1999_11
ORD IDord-4afb1ca486ee4aac9896ef97c477944b
Source noteuspto-grants-1999_11