Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098587Generated: October 30, 2026

Potassium Permanganate → 1-tert-butyl-1H-pyrrole-3-carboxylic acid

https://huagongshe.com/reaction/1098587

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium PermanganateHCID 516875—
Reactant1-tert-Butyl-1H-pyrrole-3-carbaldehydeHCID 6485565—
ReactantSodium BisulfiteHCID 23665763—
SolventAcetoneHCID 180—
SolventPropan-2-one--water (1/1)HCID 18366337—
Product1-tert-butyl-1H-pyrrole-3-carboxylic acidHCID 5087568172.1%

Reaction Steps

To a solution of 1-tert-butyl-1H-pyrrole-3-carbaldehyde (0.339 g, 2.24 mmol) in acetone (40 mL) was added, over a 2 h period, a solution of KMnO4 (0.708 g, 4.48 mmol) in Acetone/H2O (1:1, 60 mL). After 3 h, the reaction was poured into a solution of 10% NaHSO3/1N HCl (120 mL) and the solution was extracted with DCM (3×60 mL). The combined extracts were washed with H2O (2×60 mL) and 5% NaHCO3 (3×60 mL). The bicarbonate washes were carefully acidified to pH 3 and extracted with DCM (3×60 mL). The combined organic layers were washed with brine (1×), dried (MgSO4) and concentrated afford 1-tert-butyl-1H-pyrrole-3-carboxylic acid (0.270 g, 72% yield) as a white solid. MS (ESI) m/z: 168.1 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143293B2
Source datasetuspto-grants-2012_03
ORD IDord-1851086dcc6e4dadb7e2ce9eac0cc3ec
Source noteuspto-grants-2012_03