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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131755Generated: October 26, 2026

Acetone → (R)-3-iodo-1-phenyl-1-(2-methyl-4-acetoxyphenoxy)propane

https://huagongshe.com/reaction/131755

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantPotassium IodideHCID 4875—
Reactant(R)-3-chloro-1-phenyl-1-(2-methyl-4-acetoxyphenoxy)propaneHCID 69118291—
SolventDiethyl EtherHCID 3283—
Product(R)-3-iodo-1-phenyl-1-(2-methyl-4-acetoxyphenoxy)propaneHCID 6911806870%

Reaction Steps

A mixture of (R)-3-chloro-1-phenyl-1-(2-methyl-4-acetoxyphenoxy)propane (0.200 gm, 0.63 mMol) and 15 mL acetone saturated with potassium iodide was stirred at reflux under argon overnight. The reaction mixture was poured into 50 mL diethyl ether and the resulting suspension was filtered. The filtrated was washed with saturated aqueous sodium hydrogen sulfite followed by water. The remaining organic phase was dried over magnesium sulfate and concentrated under reduced pressure to provide 0.18 gm (70%) of the desired compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07384983B2
Source datasetuspto-grants-2008_06
ORD IDord-f3535f69c6404c8e9c6ae653fae55f7e
Source noteuspto-grants-2008_06