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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482979Generated: October 30, 2026

Methyl chloroformate → Methyl 3-methyl-5,6,7,8-tetrahydroquinoline-8-carboxylate

https://huagongshe.com/reaction/482979

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroformateHCID 6586—
ReactantHCID 178506786HCID 178506786—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 3-methyl-5,6,7,8-tetrahydroquinoline-8-carboxylateHCID 12278960—

Reaction Steps

8-Lithio-5,6,7,8-tetrahydro-3-methyl-8-trimethylsilylquinoline, prepared as in Example 3, is treated with 1 equivalent of methyl chloroformate in THF at -20° C. under nitrogen. After the addition the mixture is allowed to warm to ambient temperature and the solvent removed by evaporation. The residue is dissolved in 2NHCl and washed with ether basified with Na2CO3 and extracted with chloroform. The extracts are dried and evaporated. Distillation of the residue gives the title compound as a pale yellow oil bp 120°/0.25 mm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04577022
Source datasetuspto-grants-1986_03
ORD IDord-c6f3ec75ea354bae81334f56ac1b2248
Source noteuspto-grants-1986_03