Basic information Safety Supplier Related

4-(1-PYRROLIDINYL)BENZOIC ACID

Basic information Safety Supplier Related

4-(1-PYRROLIDINYL)BENZOIC ACID Basic information

Product Name:
4-(1-PYRROLIDINYL)BENZOIC ACID
Synonyms:
  • OTAVA-BB BB7018780042
  • RARECHEM AL BE 1489
  • TIMTEC-BB SBB009596
  • 4-(1-PYRROLIDINYL)BENZOIC ACID
  • 4-PYRROLIDIN-1-YL-BENZOIC ACID
  • AKOS BB-8746
  • AKOS B022048
  • BUTTPARK 99\06-02
CAS:
22090-27-3
MF:
C11H13NO2
MW:
191.23
Product Categories:
  • Building Blocks
  • Heterocyclic Building Blocks
  • Pyrrolidines
  • Acids and Derivatives
  • Heterocycles
Mol File:
22090-27-3.mol
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4-(1-PYRROLIDINYL)BENZOIC ACID Chemical Properties

Melting point:
262-296 °C (D)
Boiling point:
376.9±25.0 °C(Predicted)
Density 
1?+-.0.06 g/cm3(Predicted)
storage temp. 
2-8°C
form 
solid
pka
4.94±0.10(Predicted)
color 
Cream
CAS DataBase Reference
22090-27-3(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26
WGK Germany 
3
Hazard Note 
Harmful
HazardClass 
IRRITANT
HS Code 
29339900
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4-(1-PYRROLIDINYL)BENZOIC ACID Usage And Synthesis

Chemical Properties

Solid

Synthesis

22090-26-2

124-38-9

22090-27-3

To the reaction flask was added 0.1 mol 1-(4-bromophenyl)pyrrolidine (reactant) and 120 mL of tetrahydrofuran (solvent), the device was sealed and stirred. Nitrogen displacement was performed to remove air and the reaction mixture was subsequently cooled to -70 °C. Under stirring, 2.5 M butyl lithium (reactant) was slowly added dropwise for 20 minutes. Next, dry carbon dioxide gas was passed to saturation. The reaction was maintained at this temperature for 2 hours. Upon completion of the reaction, the reaction solution was poured into a beaker containing 20 mL of concentrated hydrochloric acid (for pH adjustment) and 100 mL of water for hydrolysis. After separation, the aqueous phase was extracted once with 50 mL of ethyl acetate (solvent). The organic phases were combined and washed to neutrality with brine, followed by drying with anhydrous sodium sulfate (desiccant). The solvent was concentrated to give a pale yellow solid. The solid was washed twice with ethyl acetate (solvent), followed by recrystallization to give white crystals 4-(1-pyrrolidinyl)benzoic acid (product) in 90% yield and 98.0% HPLC purity.

References

[1] Patent: CN105669595, 2016, A. Location in patent: Paragraph 0121; 0122; 0123

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