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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433330Generated: November 3, 2026

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

https://huagongshe.com/reaction/1433330

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 AcOEt (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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612238B2
Source datasetuspto-grants-2009_11
ORD IDord-e39b05db42544b7d8f75575d07c29983
Source noteuspto-grants-2009_11