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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1377504Generated: October 31, 2026

Potassium Iodide → HCID 22012178, compound

https://huagongshe.com/reaction/1377504

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantDiisopropyl EtherHCID 7914—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 3-bromopropionateHCID 68320—
Reactant1-BENZOTHIOPHEN-3(2H)-ONEHCID 10986413—
SolventAcetoneHCID 180—
ProductHCID 22012178HCID 220121781.3%

Reaction Steps

A mixture of benzo[b]thiophen-3-one (30 g), ethyl 3-bromopropionate (73 g), potassium carbonate (55 g), potassium iodide (1.3 g) and acetone (600 ml) was refluxed for 18 h. Filtration and removal of solvent in vacuo a red oil which was dissolved in ether (200 ml) and dried over magnesium sulfate. The ether solution was added dropwise to a suspension of lithium aluminium hydride (5 g) in ether (100ml) followed by reflux for 1 h. Usual work-up gave a viscous oil which was applied to a silica gel Column (eluent:isopropyl ether) giving 3-(benzo[b]thiophen-3-yloxy)-1-propanol (0.54 g) as an oil. The title compound was obtained according to the method described in EXAMPLE 2 using spiro[isobenzofuran-1(3H),4'-piperidine] and crystallized as the maleate salt from an acetone/ether mixture by addition of maleic acid. Yield: 0.34 g, mp: 116°-17° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665725
Source datasetuspto-grants-1997_09
ORD IDord-ba7fa1523ac94b3594361a66d32209ac
Source noteuspto-grants-1997_09