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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1089658Generated: October 30, 2026

Sodium Iodide → 6-((2,5-Dioxopyrrolidin-1-yl)oxy)-6-oxohexanoic acid

https://huagongshe.com/reaction/1089658

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantMethyl 6-[(2,5-dioxopyrrolidin-1-yl)oxy]-6-oxohexanoateHCID 4458286—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product6-((2,5-Dioxopyrrolidin-1-yl)oxy)-6-oxohexanoic acidHCID 1205228975.2%

Reaction Steps

A solution of methyl succinimidyl adipate (4.5 g, 17.5 mmol), chlorotrimethylsilane (11.1 ml, 87.5 mmol) and sodium iodide (13.1 g, 87.5 mmol) in 10 ml of acetonitrile was heated at reflux for 12 hours. The mixture was then cooled to room temperature and diluted with ethyl acetate. The reaction mixture was washed repeatedly with 5 percent aqueous sodium bisulfite until the organic solution was colorless. Then it was washed with brine, dried over anhydrous magnesium sulfate, filtered and concentrated to provide 3.2 g (71 percent yield by weight) of adipic acid monosuccinimidyl ester as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05079152
Source datasetuspto-grants-1992_01
ORD IDord-b421e2ead8834c3facc6be62830614a1
Source noteuspto-grants-1992_01