HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Permanganate → 1-tert-butyl-1H-pyrrole-3-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Permanganate | HCID 516875 | — |
| Reactant | 1-tert-Butyl-1H-pyrrole-3-carbaldehyde | HCID 6485565 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Propan-2-one--water (1/1) | HCID 18366337 | — |
| Product | 1-tert-butyl-1H-pyrrole-3-carboxylic acid | HCID 50875681 | 72.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08143293B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-1851086dcc6e4dadb7e2ce9eac0cc3ec |
| Source note | uspto-grants-2012_03 |