HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 747260Erstellt: 25. Oktober 2026
Arsenic Acid → 8-Methylquinoline-7-carboxylic acid
https://huagongshe.com/reaction/747260
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Arsenic Acid | HCID 234 | — |
| Edukt | Glycerol | HCID 753 | — |
| Edukt | Sulfuric Acid | HCID 1118 | — |
| Edukt | 3-Amino-2-methylbenzoic acid | HCID 2733699 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Produkt | 8-Methylquinoline-7-carboxylic acid | HCID 59749565 | 52,1% |
Reaktionsschritte
A mixture of 3-amino-2-methylbenzoic acid (Intermediate M1) (6.06 g, 39.6 mmol) (commercially available from Aldrich) and arsenic acid (H5As3O10) 7.43 g (commercially available from VWR/ALFA) in glycerol (5.8 mL, 79.2 mmol), and sulfuric acid (9 mL) was heated to 160° C. for 5 h. The mixture was cooled to rt, diluted with water and filtered through a bed of diatomaceous earth. The pH was adjusted to pH 6-7 with 2 M NaOH. The aqueous layer was exhaustively extracted with CHCl3:MeOH (3:1). The organic fractions were pooled and evaporated under vacuum to give a solid. This solid was titurated with CHCl3, and collected on a glass frit. The solid material was washed with hexanes and dried under high vacuum to give a pure solid, 8-methylquinoline-7-carboxylic acid (Intermediate M2) 3.86 g (51%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07396849B2 |
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| Quelldatensatz | uspto-grants-2008_07 |
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| ORD ID | ord-ecbd716e0c1642cb9e281008a2f42660 |
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| Quellennotiz | uspto-grants-2008_07 |
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