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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1687553Generated: October 30, 2026

Potassium Iodide → HCID 67264526, compound

https://huagongshe.com/reaction/1687553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium CarbonateHCID 10340—
ReactantDimethylamine, hydrochlorideHCID 10473—
ReactantPotassium CarbonateHCID 11430—
Reactant3-(3-Chloro-propyl)-8-methoxy-1,3-dihydro-benzo[d]azepin-2-oneHCID 20433769—
SolventAcetonitrileHCID 6342—
ProductHCID 67264526HCID 67264526—

Reaction Steps

Into a 1-neck round-bottom flask was added 3-(3-chloro-propyl)-8-methoxy-1,3-dihydro-benzo[d]azepin-2-one (2.5 g, 0.0094 mol), dimethylamine hydrochloride (1.534 g, 0.01882 mol), Potassium iodide (0.468 g, 0.00282 mol), and Potassium carbonate (5.201 g, 0.03763 mol), in Acetonitrile (25 mL), and the reaction was stirred over night at 50° C. The reaction mixture was next partitioned between water and dichloromethane, and the layers were separated. The aqueous phase was extracted once with dichloromethane and the combined organic extract was washed with water. The organic solution was next extracted twice with 100 mL HCl solution (˜4N), and the aqueous extract was washed once with dichloromethane (50 mL). The aqueous solution of the chlorohydrate thus obtained was basified with solid Na2CO3 to pH 11. Extraction with dichloromethane, drying of the extracts (MgSO4), concentration and high vacuum drying provided 3-(3-dimethylamino-propyl)-8-methoxy-1,3-dihydro-benzo[d]azepin-2-one, which was used without further purification (oil, 1.13 g, 44%). LC/MS (ESI+) 275 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148391B2
Source datasetuspto-grants-2012_04
ORD IDord-43f933959e6a458bae1049b9315c0343
Source noteuspto-grants-2012_04