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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 557808Generated: October 30, 2026

Sodium Iodide → 1'-Benzylspiro[1,2-benzisothiazole-3,3'-pyrrolidine]1,1-dioxide

https://huagongshe.com/reaction/557808

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantAcetonitrileHCID 6342—
ReactantChlorotrimethylsilaneHCID 6397—
Reactant2-(1-benzyl-3-hydroxypyrrolidin-3-yl)-N-(tert-butyl)benzenesulfonamideHCID 66661626—
Product1'-Benzylspiro[1,2-benzisothiazole-3,3'-pyrrolidine]1,1-dioxideHCID 6666210260.1%

Reaction Steps

To a solution of 2-(1-benzyl-3-hydroxypyrrolidin-3-yl)-N-(tert-butyl)benzene sulfonamide (350 mg, 0.00090 mol) in acetonitrile (15 mL, 0.29 mol) were added sodium iodide (418 mg, 0.00279 mol) and chlorotrimethylsilane (0.354 mL, 0.00279 mol). The reaction mixture was refluxed under nitrogen for 1 hour and then cooled down to room temperature, then quenched with 10% aqueous sodium thiosulfate solution (10 mL), and then extracted with EtOAc. The organic phase was washed with water then brine, and then dried over MgSO4 followed by filtration. The filtrate was concentrated to give the desired compound (170 mg, 60% yield). MS (ESI): 315.0 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08058288B2
Source datasetuspto-grants-2011_11
ORD IDord-9e2b0e745b9e4b4f9ec8577b4fae9964
Source noteuspto-grants-2011_11