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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 67898Generated: October 30, 2026

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

https://huagongshe.com/reaction/67898

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantN-(2-Thioacetyl-3-chlorobenzoyl)-N-cyclopentylglycine t-butyl esterHCID 20440238—
SolventAcetonitrileHCID 6342—
ProductN-(2-Thioacetyl-3-chlorobenzoyl)-N-cyclopentylglycineHCID 20440237—

Reaction Conditions

Temperature55 °C

Reaction Steps

N-(2-Thioacetyl-3-chlorobenzoyl)-N-cyclopentylglycine t-butyl ester (20.6 g, 0.05 mol) 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 The aqueous layer was quickly withdrawn and the organic layer washed 2×75 ml H2O, 2×75 ml Na2S2O3 and 2×75 ml brine.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 numberUS04347246
Source datasetuspto-grants-1982_08
ORD IDord-4ef6e783f3ae49f0b663a86b8846523c
Source noteuspto-grants-1982_08