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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437461Generated: October 27, 2026

Carbon Dioxide → 2-Methyl-5,6,7,8-tetrahydroquinoline-8-carboxamide

https://huagongshe.com/reaction/437461

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
Reactant5,6,7,8-Tetrahydro-2-methylquinolineHCID 12229420—
ReactantMethyl-2-methyl-5,6,7,8-tetrahydroquinoline-8-carboxylateHCID 12278958—
ReactantMethyl 5,6,7,8-tetrahydroquinoline-2-acetateHCID 20358396—
ReactantHCID 178506676HCID 178506676—
Product2-Methyl-5,6,7,8-tetrahydroquinoline-8-carboxamideHCID 1227896830%

Reaction Steps

Reaction of 2-methyl-5,6,7,8-tetrahydroquinoline with phenyl lithium and carbon dioxide followed by esterification according to the general method described in Examples 1B and 6B gave an inseparable mixture of methyl-2-methyl-5,6,7,8-tetrahydroquinoline-8-carboxylate and methyl 5,6,7,8-tetrahydroquinoline-2-acetate which was converted without purification to a mixture of 2-methyl-5,6,7,8-tetrahydroquinoline-8-carboxamide and 5,6,7,8-tetrahydroquinoline-2-acetamide by reaction with ammonia using the method described in Example 2. Fractional recrystallisation from diisopropyl ether gave the title compound as colourless needles m.p. 114° (overall yield 30%) (Found: C, 69.31, H, 7.45, N, 14.7, C11H14N2O requires: C, 69.45, H, 7.42; N, 14.72%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04031102
Source datasetuspto-grants-1977_06
ORD IDord-5cb3c1028d574efb9b4bd510b9e45976
Source noteuspto-grants-1977_06