1-Butylpyrrolidine

1-Butylpyrrolidine
  • CAS No.:767-10-2
Other grades of this product :
1-Butylpyrrolidine Basic information
Product Name:1-Butylpyrrolidine
Synonyms:N-BUTYL PYRROLIDINE;1-BUTYLPYRROLIDINE;1-BUTYLPYRROLIDINE FOR SYNTHESIS;1-butyl-pyrrolidin;N-butyl-Tetrahydropyrrole;Pyrrolidine, 1-butyl-
CAS:767-10-2
MF:C8H17N
MW:127.23
EINECS:212-179-4
Product Categories:API intermediates;Building Blocks;Heterocyclic Building Blocks;Pyrrolidines;Building Blocks;C4 to C10;Chemical Synthesis;Heterocyclic Building Blocks
Mol File:767-10-2.mol
1-Butylpyrrolidine Chemical Properties
Boiling point 155-157 °C/754 mmHg (lit.)
density 0.814 g/mL at 25 °C (lit.)
refractive index n20/D 1.44(lit.)
Fp 97 °F
storage temp. Refrigerator, Under inert atmosphere
solubility Chloroform (Sparingly), Ethyl Acetate (Slightly)
form Oil
color Colourless
CAS DataBase Reference767-10-2(CAS DataBase Reference)
NIST Chemistry Reference1-Butylpyrrolidine(767-10-2)
Safety Information
Hazard Codes T
Risk Statements 10-24/25
Safety Statements 16-36/37-45
RIDADR UN 2929 6.1/PG 2
WGK Germany 2
RTECS UX9800000
HazardClass 3.2
PackingGroup III
MSDS Information
ProviderLanguage
1-Butylpyrrolidine English
SigmaAldrich English
1-Butylpyrrolidine Usage And Synthesis
Uses1-Butylpyrrolidine can be used in the composition for alcohol recovery solution.
Uses1-Butylpyrrolidine has been used in:microwave-assisted synthesis of ionic liquid precursor, 1-butyl-1-methylpyrrolidinium methylcarbonate.[N,N-methylbutylpyrrolidinium] thiosalicylate, ionic liquid.The reaction of 1-butylpyrrolidine with dimethyl carbonate to yield the ionic liquid precursor, 1-butyl-1-methylpyrrolidinium methylcarbonate, has been investigated under microwave heating conditions and the reaction parameters optimised to achieve 100% yield of the pyrrolidinium salt with no by-products in under 1h.
PreparationThe synthesis of 1-butylpyrrolidine and its derivatives (1-butylpyrrolidine with a little of 1-butenylpyrrolidines) was developed via a one-pot method from ammonia and 1,4-butandiol. Here, the product of 1-butylpyrrolidine was emphatically investigated, and the yield was 76% under the optimized conditions. Such a route was realized through successive N-alkylation using aqueous ammonia as the nitrogen source over the CuNiPd/ZSM-5 catalyst, which was prepared by a simple incipient wetness method. In this route, 1,4-butandiol not only participated in the formation of the N-heterocycle, but also acted as an alkylating reagent. This work offers a straightforward, economical route for 1-butylpyrrolidine and its derivatives.One-pot synthesis of 1-butylpyrrolidine and its derivatives from aqueous ammonia and 1,4-butandiol over CuNiPd/ZSM-5 catalysts

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