Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1477188Generated: November 3, 2026

Acetic Acid → Dimethyl-(8-phenyl-1,4-dioxa-spiro[4.5]dec-8-ylmethyl)-amine

https://huagongshe.com/reaction/1477188

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantFormaldehydeHCID 712—
Reactant(8-Phenyl-1,4-dioxaspiro[4.5]decan-8-YL)methanamineHCID 20596179—
ReactantCID 101953985HCID 101953985—
SolventAcetonitrileHCID 6342—
SolventChloroform methanolHCID 21584188—
ProductDimethyl-(8-phenyl-1,4-dioxa-spiro[4.5]dec-8-ylmethyl)-amineHCID 45026964—

Reaction Steps

The title compound of step 4 (5.40 g, 21.8 mmol) was dissolved in acetonitrile (150 mL), and a cloudy solution was formed. Aqueous 37% formalin solution (30.6 mL, 407 mmol) was added. The batch was stirred for 20 min at RT and then mixed with sodium cyanoboron hydride (5.76 g, 91.7 mmol). The reaction was followed by DC in chloroform/methanol (9:1). After 4 h the solution was adjusted to pH 7 with acetic acid and concentrated to low volume in a vacuum. The residue was taken up in chloroform, washed with NaHCO3 solution and the aqueous phase extracted with ether. The combined organic phases were dried over Na2SO4 and concentrated to low volume in a vacuum. The raw product was purified by flash chromatography with chloroform/methanol (50:1→20:1→9:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403767B2
Source datasetuspto-grants-2016_08
ORD IDord-2eb16ab579144b7280e4e3b2bfdeded0
Source noteuspto-grants-2016_08