ChemicalBook CAS DataBase List 8-Hydroxyquinaldine

8-Hydroxyquinaldine synthesis

11synthesis methods

Product Name:8-Hydroxyquinaldine
CAS Number:826-81-3
Molecular formula:C10H9NO
Molecular Weight:159.18

8-hydroxyquinaldine is obtained from the reaction of 2-aminophenol with crotonaldehyde. Mix 2-aminophenol and 2-Nitrophenol homogeneously and add hydrochloric acid. Add crotonaldehyde under stirring. Heat for 6h and leave overnight. Distill the reacted o-nitrophenol by water distillation, and add sodium hydroxide solution to the residual solution to make it weakly basic. Then add powdered carbonyls for saturation, and distill 8-Hydroxyquinaldine by water distillation, and then distill the crude product under reduced pressure and recrystallize it with ethanol to obtain 8-hydroxyquinaldine.

3033-80-5
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$26.00/250mg

826-81-3
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$11.00/25g

Yield:826-81-3 76%

Reaction Conditions:

with hydrogen bromide for 36 h;Inert atmosphere;Reflux;

Steps:

1. General procedure for synthesis of 8-hydroxyquinolines 6a and 15

General procedure: To a 50 mL round-bottom flask was sequentially added o-anisidine (1.13 mL, 10.0 mmol), 3.6 mL concentrated sulfuric acid, and 15 milligrams sodium iodide and the reaction was then heated to 110°C. The respective enone/enal reagent (1.7 equivalents, 16.6 mmol) was added dropwise over 2 hours and allowed to react for an additional 4 hours. After that time, the reaction was allowed to cool to room temperature, and transferred to a separatory funnel containing 62 mL of an aqueous 1 M solution of sodium carbonate. The mixture was then extracted with dichloromethane (5 x 80 mL) and the organic layers were combined and further extracted with 12 M hydrochloric acid (5 x 50 mL). The resulting aqueous extracts were combined and neutralized with 8 M sodium hydroxide (350 mL) before being extracted with dichloromethane. The organic layers were combined and dried with anhydrous sodium sulfate, filtered and concentrated in vacuo to afford the crude product which was taken on to the next step without purification. To a 100 mL round-bottom flask was added crude methoxyquinoline intermediates (9 mmol) and 18 mL of concentrated (i.e., 48 %) hydrobromic acid. The reaction was heated to reflux for 36 hours. After this time, the reaction was allowed to cool to room temperature, transferred to a separatory funnel where the reaction was neutralized with 8 M sodium hydroxide and extracted with dichloromethane. The organic extracts were combined, filtered and concentrated in vacuo and passed through a 1-inch plug of silica gel (eluting with dichloromethane). Solvent was removed in vacuo to afford 6a (33%, 71.6 milligrams, white solid) and 15 (76%, 1.09 g, light brown solid).

References:

Abouelhassan, Yasmeen;Garrison, Aaron T.;Burch, Gena M.;Wong, Wilson;Norwood, Verrill M.;Huigens, Robert W. [Bioorganic and Medicinal Chemistry Letters,2014,vol. 24,# 21,p. 5076 - 5080] Location in patent:supporting information