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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 352858Generated: October 26, 2026

Triethylamine → 2-tert-butyl 6-methyl 3,4-dihydroisoquinoline-2,6(1H)-dicarboxylate

https://huagongshe.com/reaction/352858

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTert-butyl 6-(trifluoromethylsulfonyloxy)-3,4-dihydroisoquinoline-2(1H)-carboxylateHCID 10091216—
Catalystpalladium(II) acetateHCID 167845—
SolventMethanolHCID 887—
Product2-tert-butyl 6-methyl 3,4-dihydroisoquinoline-2,6(1H)-dicarboxylateHCID 11483176—

Reaction Conditions

Temperature70 °C

Reaction Steps

In methanol (50 ml), 2-tert-butoxycarbonyl-6-trifluoromethanesulfonyloxy-1,2,3,4-tetrahydroisoquinoline (1.34 g) was dissolved, followed by the addition of triethylamine (0.73 ml), palladium (II) acetate (40 mg) and 1,3-(diphenylphosphino)propane (145 mg). Under a carbon monoxide gas stream, the resulting mixture was stirred overnight at 70° C. The reaction mixture was concentrated under reduce pressure and the residue was purified by chromatography on a silica gel column (hexane:ethyl acetate=15:1), whereby the title compound (665 mg, 65%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06747023B1
Source datasetuspto-grants-2004_06
ORD IDord-86ed57b63d424d6cae3a36825d3afd5a
Source noteuspto-grants-2004_06