2-Bromoquinoline-4-carboxylic acid

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Company Name: SHENZHEN REISCH BIOTECH CO., LTD  Gold
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2-Bromoquinoline-4-carboxylic acid manufacturers

2-Bromoquinoline-4-carboxylic acid Basic information
Product Name:2-Bromoquinoline-4-carboxylic acid
Synonyms:4-Quinolinecarboxylic acid, 2-bromo-;2-Bromoquinoline-4-carboxylic acid
CAS:15733-87-6
MF:C10H6BrNO2
MW:252.06
EINECS:
Product Categories:
Mol File:15733-87-6.mol
2-Bromoquinoline-4-carboxylic acid Structure
2-Bromoquinoline-4-carboxylic acid Chemical Properties
Melting point 175-176 °C(Solv: ethanol (64-17-5))
Boiling point 394.7±27.0 °C(Predicted)
density 1.732±0.06 g/cm3(Predicted)
storage temp. Inert atmosphere,Room Temperature
pka2.17±0.10(Predicted)
AppearanceOff-white to gray Solid
InChIInChI=1S/C10H6BrNO2/c11-9-5-7(10(13)14)6-3-1-2-4-8(6)12-9/h1-5H,(H,13,14)
InChIKeyLUHABDKNXNXNTO-UHFFFAOYSA-N
SMILESN1C2C(=CC=CC=2)C(C(O)=O)=CC=1Br
Safety Information
HS Code 2933499090
MSDS Information
2-Bromoquinoline-4-carboxylic acid Usage And Synthesis
Synthesis
2-Hydroxy-4-quinolincarboxylic acid

15733-89-8

2-BROMOQUINOLINE-4-CARBOXYLIC ACID

15733-87-6

General procedure for the synthesis of 2-bromoquinoline-4-carboxylic acid from 2-quinolone-4-carboxylic acid: a mixture of 2-hydroxyquinoline-4-carboxylic acid (4.0 g, 21.2 mmol) and phosphorus tribromide (25.0 g, 87.2 mmol) in toluene (40 mL) was heated and refluxed for 3 hours at 100°C. Upon completion of the reaction, the mixture was cooled to room temperature and carefully poured into crushed ice. The mixture was extracted with ethyl acetate (2 x 250 mL), the organic phases were combined, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was dissolved in 1N sodium hydroxide solution (150 mL) and extracted with ethyl acetate (2 x 100 mL). The aqueous phase was adjusted to pH 3 with 1N hydrochloric acid and a white solid was precipitated. The solid was collected by filtration, washed with water and dried to give 2-bromoquinoline-4-carboxylic acid (3.0 g, 56% yield) as a white solid.

References[1] Patent: WO2006/69063, 2006, A1. Location in patent: Page/Page column 98
[2] Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 23, p. 589
[3] Patent: EP2325181, 2011, A1. Location in patent: Page/Page column 61
2-Bromoquinoline-4-carboxylic acid Preparation Products And Raw materials
Raw materials2-Hydroxy-4-quinolincarboxylic acid-->Toluene-->Phosphorus oxybromide
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