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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016802Generated: October 30, 2026

Iodine → HCID 21406153, compound

https://huagongshe.com/reaction/1016802

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant2-EthylphenolHCID 6997—
CatalystCupric ChlorideHCID 24014—
SolventChlorobenzeneHCID 7964—
ProductHCID 21406153HCID 21406153—

Reaction Steps

A solution of 119.9 ml of 2-ethylphenol in 500 ml of chlorobenzene was treated with 126.9 g of iodine and 134.5 g of copper(II) chloride and stirred under reflux for 5.5 hours. After cooling the reaction mixture was filtered and the residue was washed with methylene chloride. The combined filtrates were washed with aqueous sodium thiosulphate solution and ice-water. The organic phases were dried over sodium sulphate and concentrated. The residue was crystallized from hexane and gave 79.3 g of 2-ethyl-4-iodo-phenol. The mother liquor was chromatographed over silica gel and gave a further 41 g of 2-ethyl-4-iodo-phenol; MS (EI) m/z 248 (M).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06476264B2
Source datasetuspto-grants-2002_11
ORD IDord-73c1d6e5a8ae4415ba564ea407375f4c
Source noteuspto-grants-2002_11