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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1267885Generated: October 26, 2026

1-(2-Chloroethoxy)-2-iodo-4-(trifluoromethoxy)benzene → 1-(Vinyloxy)-2-iodo-4-(trifluoromethoxy)benzene

https://huagongshe.com/reaction/1267885

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Chloroethoxy)-2-iodo-4-(trifluoromethoxy)benzeneHCID 10904642—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
Product1-(Vinyloxy)-2-iodo-4-(trifluoromethoxy)benzeneHCID 1100202569.7%

Reaction Steps

To 1-(2-chloroethoxy)-2-iodo-4-(trifluoromethoxy)benzene (Description 10; 12.1 g, 33 mmol) in tetrahydrofuran (50 mL) at −5° C. was slowly added potassium tert-butoxide (3.7 g, 33 mmol). After addition was complete, the solution was allowed to stir to room temperature for 20 hours, and was then quenched with water (100 mL). The mixture was extracted with 50% diethyl ether/hexane (2×100 mL) and the extracts dried (MgSO4). Concentration gave an oil which was purified by silica chromatography to give the title compound as an oil (7.62 g, 23 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06555552B2
Source datasetuspto-grants-2003_04
ORD IDord-171dee239f3f4c419214631580bdf566
Source noteuspto-grants-2003_04