Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325495Generated: October 30, 2026

Sodium Iodide → N-(2-Acetylthio-3-chlorobenzoyl)-N-cyclopentylglycine

https://huagongshe.com/reaction/325495

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantN-(2-Acetylthio-3-chlorobenzoyl)-N-cyclopentylglycine t-butyl esterHCID 13420406—
SolventAcetonitrileHCID 6342—
ProductN-(2-Acetylthio-3-chlorobenzoyl)-N-cyclopentylglycineHCID 13051352—

Reaction Conditions

Temperature55 °C

Reaction Steps

N-(2-Acetylthio-3-chlorobenzoyl)-N-cyclopentylglycine t-butyl ester (20.6 g, 0.05 mole) was dissolved in 150 ml CH3CN. Sodium iodide (11.3 g, 0.075 m) was then added. The resulting slurry was covered with nitrogen and warmed to 55° C. Chlorotrimethylsilane (8.15 g, 0.075 m) was then added in one portion. The reaction was stirred 30 minutes at 55° C. under nitrogen atmosphere. The heat source was removed and the reaction cooled to room temperature in an ice bath. Water (60 ml) and CH2Cl2 (100 ml) were then added. The aqueous layer was quickly withdrawn and the organic layer washed 2×75 ml H2O, 2×75 ml Na2S2O3 and 2×75 ml brine. The organic layer was then dried (MgSO4), filtered and concentrated to yield a dark yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04440941
Source datasetuspto-grants-1984_04
ORD IDord-9f19dcdd6ea1493d8e96452c3d9b7390
Source noteuspto-grants-1984_04