Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 974752Generated: October 29, 2026

Bromocyclopentane → 2,4,6-Triiodophenoxycyclopentane

https://huagongshe.com/reaction/974752

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromocyclopentaneHCID 8728—
ReactantPotassium CarbonateHCID 11430—
Reactant2,4,6-TriiodophenolHCID 11862—
SolventDimethylformamideHCID 6228—
Product2,4,6-TriiodophenoxycyclopentaneHCID 15343323107.9%

Reaction Conditions

Temperature130 °C

Reaction Steps

Milled, anhydrous potassium carbonate (14.2 g, 103 mmol, 1.2 eq) was added in portions to a stirred solution of 2,4,6-triiodophenol (40.5 g, 85.8 mmol) in 50 ml of dry (4A sieves) dimethylformamide at room temperature. After stirring for 20 minutes, cyclopentyl bromide (12 ml, 112 mmol, 1.3 eq) in dimethylformamide (20 ml) was added and the viscous mixture was gradually heated to 130° C. under argon for approximately 45 minutes. After cooling, the mixture was filtered and the collected solid was washed with chloroform. The filtrate was concentrated in vacuo to give 50 g of an amber oil The crude oily product was partitioned between ethyl acetate (300 ml) and water (500 ml); the organic layer was dried over magnesium sulfate and passed through a short pad of silica gel. The filtrate was treated with decolorizing carbon, filtered, and stripped to give an amber oil. The oil was dried at 60° C. under high vacuum to give 40.4 g (87%) of product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05607660
Source datasetuspto-grants-1997_03
ORD IDord-9a7b41ecd0d0468b88bb621b5c57012c
Source noteuspto-grants-1997_03