HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 349033Erstellt: 25. Oktober 2026
Potassium Hydroxide → 1-Butyl-1,2,3,4-tetrahydroquinoline-7-carboxylic acid
https://huagongshe.com/reaction/349033
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | Methyl 1-butyl-1,2,3,4-tetrahydroquinoline-7-carboxylate | HCID 21086131 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 1-Butyl-1,2,3,4-tetrahydroquinoline-7-carboxylic acid | HCID 21085165 | 94,6% |
Reaktionsschritte
To a stirred solution of methyl 1-butyl-1,2,3,4-tetrahydroquinoline-7-carboxylate (156 mg, 0.63 mmol) in methanol (1.3 mL) was added potassium hydroxide (6.3 mL of a 1 M solution in water, 6.3 mmol). The reaction mixture was stirred at room temperature for 48 h and concentrated under reduced pressure. The residue was diluted with water and washed with ethyl acetate. The aqueous layer was acidified to pH 4 with 1 N hydrochloric acid and extracted with chloroform (4×100 mL). The combined organic extracts were dried (sodium sulfate), filtered, and concentrated under reduced pressure. Purification by flash column chromatography (silica, 1:9 methanol/chloroform) afforded 1-butyl-1,2,3,4-tetrahydroquinoline-7-carboxylic acid (139 mg): ESI MS m/z 234 [M+H]+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US07176242B2 |
|---|
| Quelldatensatz | uspto-grants-2007_02 |
|---|
| ORD ID | ord-47a1a3aedd774fc1a74f03771b792dea |
|---|
| Quellennotiz | uspto-grants-2007_02 |
|---|