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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437465Generated: October 30, 2026

Formamide → 3-Methyl-5,6,7,8-tetrahydroquinoline-8-carboxamide

https://huagongshe.com/reaction/437465

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormamideHCID 713—
ReactantHexaneHCID 8058—
ReactantSodium MethoxideHCID 10942334—
ReactantMethyl 3-methyl-5,6,7,8-tetrahydroquinoline-8-carboxylateHCID 12278960—
SolventHydrochloric AcidHCID 313—
Product3-Methyl-5,6,7,8-tetrahydroquinoline-8-carboxamideHCID 12278227—

Reaction Steps

A mixture of methyl-3-methyl-5,6,7,8-tetrahydroquinoline-8-carboxylate (25 g., 0.13 m), formamide (11.6, 0.26 m) and sodium methoxide (from 2.99 g., 0.13m sodium) was heated with stirring in an oil bath at 120° for 1 hour. The reaction mixture was further heated at 100° for 3 hours under reduced pressure (15 mm Hg). The cooled reaction mixture was diluted with 2N HCl to give an acidic solution which was extracted with ethylacetate (2 × 50 ml.) and the combined extracts discarded. The aqueous solution was adjusted to pH 9.0 with solid Na2CO3, saturated with NaCl and extracted with chloroform (3 × 100 ml.). The combined extracts were dried and evaporated to give a pale yellow oil which solidified on trituration with n-hexane. Recrystallisation from ethylacetate gave the title compound as colourless cubes (18.6 g., 88%) m.p. 110°. Found: C, 69.6; H, 7.4; N, 14.4%. C11H14N2O requires: C, 69.5; H, 7.4; N, 14.7%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04031102
Source datasetuspto-grants-1977_06
ORD IDord-bef56dbdc5b6460d9c8c7519cd5d0a5b
Source noteuspto-grants-1977_06