Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1008257Generated: October 25, 2026

Trimethylsilyl iodide → 4-(4Iodo-1-oxobutyl)-alpha,alpha-dimethylphenylacetic acid

https://huagongshe.com/reaction/1008257

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl iodideHCID 85247—
Reactant4-(Cyclopropylcarbonyl)-I+-,I+--dimethylbenzeneacetic acidHCID 9856066—
ReactantSodium BisulfiteHCID 23665763—
SolventDichloromethaneHCID 6344—
Product4-(4Iodo-1-oxobutyl)-alpha,alpha-dimethylphenylacetic acidHCID 1131438277.4%

Reaction Steps

A solution of 10.5 g of 4-(cyclopropyl-oxo-methyl)-α,α-dimethylphenylacetic acid, prepared in accordance with Example 2, in 250 mL of CH2Cl2 was cooled in an ice-MeOH bath and 25 g of trimethylsilyliodide was then added rapidly via pipette. The mixture was stirred in the ice bath for one hour, warmed to ambient temperature, and stirred for one hour. A solution of aqueous sodium bisulfite was then added and the mixture was stirred well. The phases were partitioned and the aqueous layer was extracted with CH2Cl2. The combined organics were washed with saturated aqueous NaCl, dried over MgSO4 filtered, and concentrated in vacuo to afford 12.6 g (77%) of 4-(4-iodo-1-oxobutyl)-α,α-dimethylphenylacetic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06797826B2
Source datasetuspto-grants-2004_09
ORD IDord-56e3cfaa7e0345cdb244be905f27a58e
Source noteuspto-grants-2004_09