Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 706896Erstellt: 25. Oktober 2026

Hexamethylphosphoramide → Ethyl 2-hydroxy-6,6-dimethylcyclohex-1-enecarboxylate

https://huagongshe.com/reaction/706896

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHexamethylphosphoramideHCID 12679—
Edukt3-Methyl-2-cyclohexen-1-oneHCID 14511—
EduktEthyl cyanoformateHCID 69336—
EduktHCID 178418348HCID 178418348—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
LösungsmittelWaterHCID 962—
LösungsmittelDiethyl EtherHCID 3283—
ProduktEthyl 2-hydroxy-6,6-dimethylcyclohex-1-enecarboxylateHCID 67126375—

Reaktionsbedingungen

Temperatur-5 °C

Reaktionsschritte

Into a 500 mL flame dried round-bottomed flask was added copper(I) iodide (18 g) in ether (200 mL) to give a suspension. After cooling to −5° C., methyllithium (120 mL, 1.6M in ether) was added dropwise. After stirring at −5° C. for 1 hour, 3-methylcyclohex-2-enone (5.15 mL) in 15 ml ether was added dropwise, and the mixture was stirred at −5° C. for 1 hour. After cooling to −78° C., hexamethylphosphoramide (60 mL) was added dropwise. Ethyl carbonocyanidate (23.74 mL) was added. After stirring at −78° C. for 20 minutes, the mixture was warmed up to room temperature, and stirred for 1 hour. The mixture was poured into cold water, and the layers were separated. The aqueous layer was extracted with ether (3×20 mL). The combined organic layers were washed with saturated aqueous NH4Cl (3×20 mL), dried over Na2SO4, filtered, and dried under vacuum. The crude product was added to a silica gel column and purified by eluting with 0-10% ethyl acetate in hexane.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09174982B2
Quelldatensatzuspto-grants-2015_11
ORD IDord-fd71c6139f574343984e3b35000a0dab
Quellennotizuspto-grants-2015_11