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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503916Generated: October 26, 2026

Water → tert-Butyl 3-bromo-1H-pyrrole-1-carboxylate

https://huagongshe.com/reaction/503916

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDi-tert-butyl dicarbonateHCID 90495—
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant3-Bromo-1-(triisopropylsilyl)pyrroleHCID 2763302—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 3-bromo-1H-pyrrole-1-carboxylateHCID 6687805324.2%

Reaction Steps

A solution of TBAF (1.0 M in THF, 3.6 mL) was added to a solution of 3-bromo-1-triisopropylsilanyl-1H-pyrrole (1.0 g, 3.308 mmol) in THF (10 mL) and the mixture was stirred at room temperature for 30 minutes. (BOC)2O (0.866 g, 3.965 mmol) and DMAP (40 mg, 0.3308 mmol) were added to the reaction and the resulting mixture was stirred for 2 additional hours. Water was added, and the mixture was extracted with EtOAc. The combined organic extracts were washed with water and with brine; dried over Na2SO4, filtered, and evaporated under reduced pressure. The residue was purified via flash chromatography (hexane/EtOAc) to give 0.197 g (24% yield) of 3-bromo-pyrrole-1-carboxylic acid tert-butyl ester as a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776910B2
Source datasetuspto-grants-2010_08
ORD IDord-b7adad826d1346d2a0b9a67aa0043b68
Source noteuspto-grants-2010_08