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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1531812Generated: November 2, 2026

Boron trifluoride → 7-Methoxyisoquinoline

https://huagongshe.com/reaction/1531812

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluorideHCID 6356—
ReactantTrifluoroacetic anhydrideHCID 9845—
Reactant3-MethoxybenzaldehydeHCID 11569—
ReactantAmmonium HydroxideHCID 14923—
Product7-MethoxyisoquinolineHCID 59437572%

Reaction Steps

To a solution of BF3.AcOH complex (33.78 g, 0.180 mol) in triflouoracetic anhydride (40 ml) at 0° C. was added a solution of the imine prepared from 3-methoxybenzaldehyde and aminoethanaldiethylacetal (Tetrahedron, 1971, 27, 1253) (15.06 g, 0.0599 mol) in trifluoroacetic anhydride (40 ml), maintaining the temperature below 10° C. After 48 hours, the mixture was poured into ice-water (300 ml), the solution made basic with concentrated ammonium hydroxide and extracted with dichloromethane. The organic phase was then extracted with aqueous hydrochloric acid solution (5N, 2×400 ml). The combined aqueous was made basic with concentrated ammonium hydroxide solution and extracted with dichloromethane. The organic phase was dried (MgSO4), filtered, the solvent removed under reduced pressure and the residue purified on silica, eluting with a solvent gradient of 98:2 to 95:5 dichloromethane:methanol, to give the title compound, (6.85 g, 72%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06200978B1
Source datasetuspto-grants-2001_03
ORD IDord-6595c065076c46e0b9472a45393a7257
Source noteuspto-grants-2001_03