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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 222603Erstellt: 24. Oktober 2026

Potassium Iodide → HCID 178525739, Verbindung

https://huagongshe.com/de/reaction/222603

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium IodideHCID 4875—
EduktSodium ChlorideHCID 5234—
Edukt1,4-DichlorobutaneHCID 8059—
EduktPotassium CarbonateHCID 11430—
EduktHCID 178501209HCID 178501209—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
ProduktHCID 178525739HCID 178525739—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08207349B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-f816885f340d4f4c8e5545ee9a3fc62a
Quellennotizuspto-grants-2012_06