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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571302Generated: October 30, 2026

Potassium Iodide → HCID 86681709, compound

https://huagongshe.com/reaction/571302

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
ReactantN,N-Dimethylaminoethyl chloride hydrochlorideHCID 11636816—
ReactantHCID 86681698HCID 86681698—
SolventAcetoneHCID 180—
ProductHCID 86681709HCID 8668170941.6%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of tert-butyl 2-(5-(methylsulfonamido)-1,3-dioxoisoindolin-2-yl)acetate (600 mg, 1.693 mmol) (prepared in an analogous manner as previously described in Example 34, Scheme 34, Steps 1, 2, 3) in acetone (20 ml), 2-chloro-N,N-dimethylethanamine hydrochloride (366 mg, 2.54 mmol), potassium carbonate (468 mg, 3.39 mmol) and potassium iodide (281 mg, 1.693 mmol) were added. The resulting mixture was stirred at 50° C. for 48 hours. The insoluble inorganic salts were filtered off, and the filtrate was evaporated. The crude was purified by was crystallization from EtOH affording tert-butyl 2-(5-(N-(2-(dimethylamino)ethyl)methylsulfonamido)-1,3-dioxoisoindolin-2-yl)acetate (300 mg, 0.705 mmol, 41.6% yield, MS/ESI+ 426.0 [MH]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09024027B2
Source datasetuspto-grants-2015_05
ORD IDord-e060afaa9f93442ab93c45760df563b8
Source noteuspto-grants-2015_05