HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl chloroformate → Methyl 3-methyl-5,6,7,8-tetrahydroquinoline-8-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | HCID 178506786 | HCID 178506786 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 3-methyl-5,6,7,8-tetrahydroquinoline-8-carboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04577022 |
| Source dataset | uspto-grants-1986_03 |
| ORD ID | ord-c6f3ec75ea354bae81334f56ac1b2248 |
| Source note | uspto-grants-1986_03 |