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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1616651Generated: November 2, 2026

Hydrochloric Acid → 4-Methoxy-9-aza-tricyclo[6.3.1.0*2,7*]dodeca-2,4,6-triene

https://huagongshe.com/reaction/1616651

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-Methoxy-9-aza-tricyclo[6.3.1.0*2,7*]dodeca-2,4,6-trien-10-oneHCID 66941775—
SolventTetrahydrofuranHCID 8028—
Product4-Methoxy-9-aza-tricyclo[6.3.1.0*2,7*]dodeca-2,4,6-trieneHCID 14857735—

Reaction Conditions

Temperature-10 °C

Reaction Steps

1 M Borane tetrahydrofuran complex (70 mL) is added dropwise to a solution of 4-methoxy-9-aza-tricyclo[6.3.1.0*2,7*]dodeca-2,4,6-trien-10-one (3.0 g) in tetrahydrofuran (20 mL) chilled in an ice bath. The resulting solution is stirred at reflux temperature for 5 h and then at room temperature overnight. The solution is cooled to ca. −10° C. and half-concentrated hydrochloric acid (50 mL) is added carefully. The mixture is stirred at room temperature for 1 h and an additional hour at reflux temperature. The solvent is removed and 2 M aqueous NaOH solution (50 mL) is added to the residue. The resulting mixture is extracted with dichloromethane and the combined organic extracts are dried (MgSO4). After removal of the solvent, the residue is taken up in ethanol (20 mL) and the resulting solution is treated with oxalic acid (3 mL) to obtain the oxalate salt of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765780B2
Source datasetuspto-grants-2014_07
ORD IDord-0a6ac8828b6e4d6cbfa9dce881af23ca
Source noteuspto-grants-2014_07