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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 649272Generated: October 25, 2026

2-Methyl-1,2,3,4-tetrahydroquinoline → Hexadecane

https://huagongshe.com/reaction/649272

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-1,2,3,4-tetrahydroquinolineHCID 96289—
Reactant2-Methyldecahydroquinoline (mixture of isomers)HCID 524016—
Reactant5,6,7,8-Tetrahydro-2-methylquinolineHCID 12229420—
ProductHexadecaneHCID 11006—

Reaction Steps

The autoclave was cooled and the contents were suction filtered. Gas liquid chromatographic analysis of the colorless liquid filtrate on a 6'×1/8" 10% Carbowax 20M column at 200° C. showed that the only product of the reaction was 2-methyl-1,2,3,4-tetrahydroquinoline (96% 2-methyl-1,2,3,4-tetrahydroquinoline and 4% starting material). There were no detectable amounts of 2-methyl-5,6,7,8-tetrahydroquinoline and 2-methyldecahydroquinoline. Gas liquid chromatographic analysis with an external standard showed that the absolute yield of product based on consumed starting material was 100%. The use of cyclohexane as the solvent instead of n-hexadecane gave the same result (97% of 2-methyl-1,2,3,4-tetrahydroquinoline and 3% of 2-methylquinoline).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04739063
Source datasetuspto-grants-1988_04
ORD IDord-cef0c9a723fd45e4bfb81215512938fa
Source noteuspto-grants-1988_04