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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1643346Generated: October 26, 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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1,3,3-TetramethylguanidineHCID 66460—
ReactantLithium ChlorideHCID 433294—
Reactant4-(Benzyloxy)-3,5-dimethylbenzaldehydeHCID 563557—
ReactantDiethyl(3-oxo-1,4-dioxaspiro[4.5]dec-2-yl)-phosphonateHCID 59259703—
SolventTetrahydrofuranHCID 8028—
Solventtert-Butyl methyl etherHCID 15413—
Product(3E)-3-[[3,5-dimethyl-4-(phenylmethoxy)phenyl]methylene]-1,4-dioxaspiro[4.5]decan-2-oneHCID 59259697—

Reaction Conditions

Temperature-20 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119797B2
Source datasetuspto-grants-2012_02
ORD IDord-9878ce2dd77a4d87abaf4743b58543bc
Source noteuspto-grants-2012_02