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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648699Generated: October 30, 2026

Potassium Iodide → HCID 14127331, compound

https://huagongshe.com/reaction/648699

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant1-Bromo-3-chloropropaneHCID 8006—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 13594461HCID 13594461—
SolventAcetonitrileHCID 6342—
ProductHCID 14127331HCID 1412733181.6%

Reaction Steps

A mixture of 5.0 g of methyl 3-oxo-2,3,4,5-tetrahydro-1-benzoxepin-2-carboxylate, 7.1 g of 1-bromo-3-chloropropane, 1.5 g of potassium iodide, 6.3 g of potassium carbonate and 60 ml of acetonitrile is heated under refluxing for 4 hours. After cooling, the inorganic substances are filtered off and the filtrate is concentrated under reduced pressure. The residue is treated with water and then extracted with ethyl acetate. The organic layer is washed with water, dried, and evaporated under reduced pressure. The residue is purified by column chromatography on silica gel (eluant: hexane:ethyl acetate=8:1→2:1), to give 5.5 g of methyl 2-(3-chloropropyl)-3-oxo-2,3,4,5-tetrahydro-1-benzoxepin-2-carboxylate as a colorless oil. Recrystallization from ethanol gives 4.4 g of colorless prisms: m.p. 75°-77° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04736031
Source datasetuspto-grants-1988_04
ORD IDord-52f1a086ab2f4622b566249a7fee8229
Source noteuspto-grants-1988_04