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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1829079Generated: October 30, 2026

Sodium Iodide → HCID 22061464, compound

https://huagongshe.com/reaction/1829079

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
ReactantMorpholine, 4-(2-chloroethyl)-, hydrochloride (1:1)HCID 77210—
Reactant5-HYDROXYPHTHALIDEHCID 231886—
SolventEthanolHCID 702—
ProductHCID 22061464HCID 2206146482%

Reaction Steps

A mixture of 5-hydroxyphthalide (1.0 g, 6.66 mmol), 4-(2-chloroethyl)-morpholine hydrochloride (1.49 g, 8.01 mmol), potassium carbonate (2.3 g, 16.6 mmol) and sodium iodide (1.0 g, 6.67 mmol) in ethanol (40 ml) was stirred at reflux under nitrogen for 18 hours. The mixture was cooled to room temperature, and filtered through celite. The filtrate solution was evaporated to dryness. The residue was partitioned between EtOAc (75 ml) and 2M HCl solution (50 ml). The organic layer was extracted with 2M HCl (2×30 ml). The aqueous layers were combined, basified with NaOH aqueous solution, and extracted with CHCl3 (3×50 ml). The organic layers were combined, dried over anhydrous Na2SO4, and evaporated to a light brown solid, which was triturated with CHCl3/Hexanes to give 5-(2-morpholin-4-yl-ethoxy)-3H-isobenzofuran-1-one as white crystals (1.43 g, 82%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07060844B2
Source datasetuspto-grants-2006_06
ORD IDord-de749044d89e46b4ae1bd891cc070134
Source noteuspto-grants-2006_06