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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1906519Generated: October 31, 2026

Epichlorohydrin → HCID 20212125, compound

https://huagongshe.com/reaction/1906519

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEpichlorohydrinHCID 7835—
ReactantSodium hydrideHCID 24758—
Reactant2-Iodo-5-(trifluoromethyl)phenolHCID 13823538—
SolventDimethylformamideHCID 6228—
ProductHCID 20212125HCID 2021212586%

Reaction Conditions

Temperature60 °C

Reaction Steps

A sample of 20 g (0.069 mole) of 2-iodo-5-trifluoromethylphenol was added in portions to a suspension of 0.07 mole of NaH (from 3.36 g of 50% NaH which had been washed free of oil with hexane) in 150 ml of dry DMF under N2. When gas evolution had ceased, a 27 ml (0.347 mole) sample of epichlorohydrin was added dropwise at 5° C. The mixture was heated at 60° C. for 3 hr and allowed to stand at 25° C. for 16 hr. A precipitate was removed by filtration. The filtrate was concentrated to dryness in vacuo. The residue was taken up in ether, washed with water and brine, dried (K2CO3) and the solvent evaporated in vacuo to give 20.4 g (86% yield) of [(2-iodo-5-trifluoromethylphenoxy)methyl]oxirane as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04652584
Source datasetuspto-grants-1987_03
ORD IDord-91cbc5e5b04a4ed185c800e5fcaa4970
Source noteuspto-grants-1987_03