HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Methyl-1,2,3,4-tetrahydroquinoline → Hexadecane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Methyl-1,2,3,4-tetrahydroquinoline | HCID 96289 | — |
| Reactant | 2-Methyldecahydroquinoline (mixture of isomers) | HCID 524016 | — |
| Reactant | 5,6,7,8-Tetrahydro-2-methylquinoline | HCID 12229420 | — |
| Product | Hexadecane | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04739063 |
| Source dataset | uspto-grants-1988_04 |
| ORD ID | ord-cef0c9a723fd45e4bfb81215512938fa |
| Source note | uspto-grants-1988_04 |