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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222603Generated: October 26, 2026

Potassium Iodide → HCID 178525739, compound

https://huagongshe.com/reaction/222603

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium ChlorideHCID 5234—
Reactant1,4-DichlorobutaneHCID 8059—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 178501209HCID 178501209—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 178525739HCID 178525739—

Reaction Conditions

Temperature100 °C

Reaction Steps

1,4-Dichlorobutane (2.3 ml, 21 mmol), potassium carbonate (12.6 g, 91 mmol) and potassium iodide (400 mg) are added to a solution of methyl cis-4-aminocyclo-hexanecarboxylate hydrochloride (4 g, 21 mmol) in 32 ml of DMF and the mixture is stirred at 100° C. for 6 h and then at RT for 3 d. The reaction mixture is diluted with 200 ml of water, neutralized with glacial acetic acid, saturated with sodium chloride and extracted with dichloromethane. The organic phases are dried, filtered and evaporated. Yield: 3.8 g of methyl cis-4-(pyrrolidin-1-yl)cyclohexanecarboxylate. The intermediate is then stirred, in 10 ml of methanol, with 25 ml of sodium hydroxide solution (1 N) at RT for 15 h. After the methanol has been removed in vacuo, the reaction mixture is adjusted to pH 6 with hydrochloric acid and evaporated further. The residue is taken up in methanol and purified by filtration through silica gel. Yield: 3.5 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207349B2
Source datasetuspto-grants-2012_06
ORD IDord-f816885f340d4f4c8e5545ee9a3fc62a
Source noteuspto-grants-2012_06