Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2383046Generated: October 29, 2026

Trifluoroacetic acid → HCID 86761610, compound

https://huagongshe.com/reaction/2383046

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantAcetic AnhydrideHCID 7918—
Reactant1-TetraloneHCID 10724—
Reactant3-MethoxyphenethylamineHCID 74866—
CatalystTitanium isopropoxideHCID 11026—
SolventFormic AcidHCID 284—
ProductHCID 86761610HCID 86761610—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of tetralone (1.50 g), 3-methoxyphenethylamine (1.86 g), and titanium tetraisopropoxide (4.55 mL) was stirred under an argon atmosphere at 80° C. for 1 hour. The reaction mixture was cooled in an ice-MeOH bath. A mixture of formic acid (39 mL) and acetic anhydride (97 mL) was added to the reaction mixture under stirring at an internal temperature of 0° C. or lower. After the addition was complete, the reaction mixture was stirred at 80° C. for 2 hours, and trifluoroacetic acid (158 mL) was added thereto, followed by stirring at an internal temperature of 70° C. for 3 hours. After the reaction was complete, the mixture was cooled to room temperature and concentrated under reduced pressure. The residue was made weak alkaline by using a saturated aqueous sodium hydrogen carbonate solution and was extracted with EtOAc. The organic layer was washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane-EtOAc) to obtain 6 methoxy-3,3′,4,4′-tetrahydro-2H,2′H-spiro[isoquinoline-1,1′-naphthalene]-2-carbaldehyde (1.86 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263607B2
Source datasetuspto-grants-2012_09
ORD IDord-dd7447ec8828440da7fe717ef91901b6
Source noteuspto-grants-2012_09