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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 490066Generated: October 25, 2026

Sodium Iodide → 1-((4-(2-Iodoethyl)phenoxy)methyl)benzene

https://huagongshe.com/reaction/490066

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactantp-(Benzyloxy)phenethyl alcoholHCID 3017260—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product1-((4-(2-Iodoethyl)phenoxy)methyl)benzeneHCID 10427223—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-(4-benzyloxy-phenyl)-ethanol (78.72 g, 0.34 mol) in methylene chloride (400 ml) is added triethylamine (67.3 ml, 0.44 mol, 1.4 eq), then at 0° C. is added mesylchloride (34.8 ml, 0.44 mol, 1.3 eq). The reaction mixture is stirred at 0° C. for 30 minutes and allowed to rise to room temperature. The reaction mixture is extracted with methylene chloride (2×300 ml), the combined organic layers are then washed with brine (2×300 ml) and concentrated under vacuum. To the crude product in solution in ethyl acetate (600 ml) is added sodium iodide (67.2 g, 0.44 mol, 1.3 eq) and the reaction mixture is stirred under reflux for 6 hours. After filtration, the organic layer is washed with brine (3×400 ml), dried with Na2SO4, filtered and concentrated under vacuum. 1-Benzyloxy-4-(2-iodo-ethyl)-benzene is isolated after crystallization with diethyl ether (116.5 g, 86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07528120B2
Source datasetuspto-grants-2009_05
ORD IDord-80e18cd9d0e5467a885d546509bdecc7
Source noteuspto-grants-2009_05