N-T-BOC-PYRROLE
N-T-BOC-PYRROLE
  • CAS No.:5176-27-2
Other grades of this product :
N-T-BOC-PYRROLE Basic information
Product Name:N-T-BOC-PYRROLE
Synonyms:TERT-BUTYL PYRROL-1-CARBOXYLATE;TERT-BUTYL 1-PYRROLECARBOXYLATE;N-T-BOC-PYRROLE;N-BOC-1H-PYRROLE;tert-butyl 1H-pyrrole-1-carboxylate;tert-butyl-pyrrole-carboxylate;N-Boc-Pyrrole;1-Boc-pyrrole
CAS:5176-27-2
MF:C9H13NO2
MW:167.21
EINECS:
Product Categories:carboxylic ester;Building Blocks;Chemical Synthesis;Heterocyclic Building Blocks;Pyrroles
Mol File:5176-27-2.mol
N-T-BOC-PYRROLE Chemical Properties
Boiling point 91-92 °C20 mm Hg(lit.)
density 1 g/mL at 25 °C(lit.)
refractive index n20/D 1.4685(lit.)
Fp 167 °F
storage temp. Sealed in dry,Room Temperature
solubility Acetonitrile, Dichloromethane, Ethyl Acetate, Methanol, Tetrahydrofuran
form Solution
pka-6.10±0.70(Predicted)
color Colorless to yellow
InChIKeyIZPYBIJFRFWRPR-UHFFFAOYSA-N
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26
WGK Germany 3
HS Code 2933998090
MSDS Information
ProviderLanguage
SigmaAldrich English
N-T-BOC-PYRROLE Usage And Synthesis
Chemical PropertiesColorless liquid
UsesPyrrole-1-carboxylic Acid tert-Butyl Ester is an intermediate in the synthesis of pyrrole derived anti-cancer Agent.
UsesN-Boc-pyrrole was used in the synthesis of 1-(tert-butoxycarbonyl)-1H-pyrrol-2-ylboronic acid by treating with n-BuLi and subsequent reaction with trimethyl borate.It may be used as starting material in the synthesis of the following:
  • tropane drivatives
  • N-boc-2-(4-methoxyphenyl)pyrrole
  • N-boc-pyrrol-2-ylboronic acid
Synthesis Reference(s)The Journal of Organic Chemistry, 31, p. 764, 1966 DOI: 10.1021/jo01341a027
General DescriptionN-Boc-pyrrole is an N-protected pyrrole. It undergoes Diels–Alder reaction with enantiomerically pure allene-1,3-dicarboxylates to form endo-adducts with retention in configurations at two newly generated stereogenic centers. It also undergoes cyclopropanation with methyl phenyldiazoacetate to form both monocyclopropane and dicyclopropane. Its Ir-catalyzed C-H borylation followed by cross coupling with 3-chlorothiophene to form biheterocycle has been reported.

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