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CAS 130418-90-5

:

tert-butyl (2R)-2-ethynylpyrrolidine-1-carboxylate

Description:
Tert-butyl (2R)-2-ethynylpyrrolidine-1-carboxylate is an organic compound characterized by its pyrrolidine ring structure, which is a five-membered nitrogen-containing heterocycle. The presence of the tert-butyl group contributes to its hydrophobic nature, enhancing its solubility in organic solvents. The ethynyl substituent introduces a triple bond, which can participate in various chemical reactions, including cycloadditions and cross-coupling reactions, making it a valuable intermediate in organic synthesis. The carboxylate functional group indicates that the compound can act as an acid, and its ester form suggests it may be involved in esterification reactions. The stereochemistry at the 2-position of the pyrrolidine ring is significant, as it can influence the compound's reactivity and interaction with biological systems. Overall, this compound's unique structural features make it of interest in medicinal chemistry and synthetic organic chemistry, particularly in the development of pharmaceuticals and agrochemicals.
Formula:C11H17NO2
InChI:InChI=1/C11H17NO2/c1-5-9-7-6-8-12(9)10(13)14-11(2,3)4/h1,9H,6-8H2,2-4H3/t9-/m0/s1
SMILES:C#C[C@H]1CCCN1C(=O)OC(C)(C)C
Synonyms:
  • 1-pyrrolidinecarboxylic acid, 2-ethynyl-, 1,1-dimethylethyl ester, (2R)-
  • tert-Butyl (2R)-2-ethynylpyrrolidine-1-carboxylate
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