HuagongsheHuagongshe Chemistry Print Report · For research reference only
Quinaldic Acid → Benzyl Alcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Quinaldic Acid | HCID 7124 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Benzyl Alcohol | HCID 244 | — |
| Product | Imidazolate | HCID 3386966 | — |
Reaction Steps
The carboxylic acid functionality in the quinolinecarboxylic acid (A) is protected using standard carboxylic acid protection procedures well known in the art, e.g., by formation of the corresponding ester, to give compound (B). For example, the benzyl ester (R21 is benzyl in (B)) may be prepared by treating a solution of compound (A) in EtOAc at room temperature with 1,1′-carbonyldiimidazole to produce the activated, imidazolide derivative of (A, then adding benzyl alcohol to the reaction mixture.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07368573B2 |
| Source dataset | uspto-grants-2008_05 |
| ORD ID | ord-8080a24a10414beab4f64618a523f097 |
| Source note | uspto-grants-2008_05 |