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HRID 1643346Erstellt: 26. Oktober 2026

1,1,3,3-Tetramethylguanidine → (3E)-3-[[3,5-dimethyl-4-(phenylmethoxy)phenyl]methylene]-1,4-dioxaspiro[4.5]decan-2-one

https://huagongshe.com/reaction/1643346

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,1,3,3-TetramethylguanidineHCID 66460—
EduktLithium ChlorideHCID 433294—
Edukt4-(Benzyloxy)-3,5-dimethylbenzaldehydeHCID 563557—
EduktDiethyl(3-oxo-1,4-dioxaspiro[4.5]dec-2-yl)-phosphonateHCID 59259703—
LösungsmittelTetrahydrofuranHCID 8028—
Lösungsmitteltert-Butyl methyl etherHCID 15413—
Produkt(3E)-3-[[3,5-dimethyl-4-(phenylmethoxy)phenyl]methylene]-1,4-dioxaspiro[4.5]decan-2-oneHCID 59259697—

Reaktionsbedingungen

Temperatur-20 °C

Reaktionsschritte

4.2 g lithium chloride (0.1 Mol), 20.0 g (83.2 mmol) of 4-benzyloxy-3,5-dimethylbenzaldehyde (D) and 31.62 g (108.2 mmol) of diethyl (3-oxo-1,4-dioxaspiro[4.5]dec-2-yl)-phosphonate (C) are suspended in 130 mL tetrahydrofuran and cooled to −20° C. At this temperature 12.5 mL (0.1 Mol) tetramethylguanidine are added dropwise. After the addition has ended the suspension formed is heated to ambient temperature and stirred for 1 hour. After the addition of 190 mL tert.butyl-methylether the organic phase is washed with 150 mL water and 30 mL saturated saline solution, dried and evaporated down. The resulting yellow oil is taken up in 145 mL methanol and stirred intensively for 1 hour at −10° C., during which time a white solid is formed. The solid formed is suction filtered, washed twice with 20 mL methanol/water (1:1) and dried at 45° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08119797B2
Quelldatensatzuspto-grants-2012_02
ORD IDord-9878ce2dd77a4d87abaf4743b58543bc
Quellennotizuspto-grants-2012_02