HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → methyl quinoline-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Quinaldic Acid | HCID 7124 | — |
| Product | methyl quinoline-2-carboxylate | HCID 421738 | — |
Reaction Steps
Reaction of 10.0 g of quinaldic acid with 5.4 ml of methyliodide by the method described in Example 97f) for 20 h at room temperature and purification of the crude product by FC over 80 g of silica gel (mobile phase C) gives methyl quinaldate as a white solid: Rf (50:50:6 mixture of hexane, ethyl acetate and glacial acetic acid)=0.65.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05719141 |
| Source dataset | uspto-grants-1998_02 |
| ORD ID | ord-5d7d138d003244b081a80983a7f8f1b6 |
| Source note | uspto-grants-1998_02 |