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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1989839Generated: October 30, 2026

4-Iodophenol → HCID 58773798, compound

https://huagongshe.com/reaction/1989839

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-IodophenolHCID 10894—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 6-bromohexanoateHCID 117544—
SolventAcetoneHCID 180—
ProductHCID 58773798HCID 5877379896.4%

Reaction Steps

Ethyl 6-bromohexanoate (5.55 g, 25 mmol) in acetone (100 ml) was treated with 4-iodophenol (5.55 g, 25 mmol) and potassium carbonate (6.9 g 50 mmol). The stirred reaction was heated under reflux for 60 h. The reaction was then allowed to cool and the reaction concentrated in vacuum to a gum. The reaction was them partitioned between ethyl acetate (100 ml) and water (100 ml). The ethyl acetate layer was separated dried, over magnesium sulfate and concentrated in vacuo to give a colourless gum (8.71 g, 24.1 mmol, 96%), δH (CDCl3) 1.26 (3H, t, CO2CH2CH3), 1.46-1.81 (6H, m, 3,4,5-CH2), 2.33 (2H, t, 2-CH2), 3.91 (2H, t, 6-CH 2), 4.13 (2H, q, CO2CH2CH3), 6.66 (2H, dd, 2,6-ArH), 7.53 (2H, dd, 3,5-ArH), δH (CDCl3) 14.20, 24.60, 25.53, 28.75, 34.14, 60.20, 67.67, 82.44, 116.83,1 38.09, 158.84, and 173.52.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07642373B2
Source datasetuspto-grants-2010_01
ORD IDord-5bb9f982af6f424083486cd52587299c
Source noteuspto-grants-2010_01