477516
N-Boc-2,5-dihydro-1H-pyrrole
96%
Synonym(s):
tert-Butyl 2,5-dihydro-1H-pyrrole-1-carboxylate
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About This Item
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Quality Level
Assay
96%
refractive index
n20/D 1.458 (lit.)
bp
208 °C (lit.)
density
0.981 g/mL at 25 °C (lit.)
SMILES string
CC(C)(C)OC(=O)N1CC=CC1
InChI
1S/C9H15NO2/c1-9(2,3)12-8(11)10-6-4-5-7-10/h4-5H,6-7H2,1-3H3
InChI key
YEBDZDMYLQHGGZ-UHFFFAOYSA-N
General description
N-Boc-2,5-dihydro-1H-pyrrole, also known as tert-butyl 2,5-dihydro-1H-pyrrole-1-carboxylate, can be synthesized from N-boc-diallylamine.
Application
N-Boc-2,5-dihydro-1H-pyrrole (tert-Butyl 2,5-dihydro-1H-pyrrole-1-carboxylate) may be used in the preparation of tert-butyl 3-aryl-2,3-dihydro-1H-pyrrole-1-carboxylate.
Used in a synthesis of ß-aryl-GABA analogues by Heck arylation with arenediazonium salts.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
178.0 °F
Flash Point(C)
81.1 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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A Short and Efficient Synthesis of (S)-1-Boc-2, 5-dihydro-1H-pyrrole-2-carboxylic Acid.
Synthesis, 1, 46-48 (2001)
Synthesis of aryl pyrrolizidines from endocyclic enecarbamates. Novel applications of the Heck arylation of 3-pyrrolines using diazonium salts.
ARKIVOC (Gainesville, FL, United States), 10, 390-403 (2003)
The Journal of organic chemistry, 70(3), 1050-1053 (2005-01-29)
We report herein a new, practical, and economic synthesis of the phosphodiesterase inhibitor Rolipram on a multigram scale as well as the synthesis of new 4-aryl pyrrolidones and beta-aryl-gamma-amino butyric acids (GABA derivatives) employing an efficient Heck-Matsuda arylation of 3-pyrroline
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