HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638696Generated: October 29, 2026
Potassium Hydroxide → HCID 57894353, compound
https://huagongshe.com/reaction/638696
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 86618067 | HCID 86618067 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 57894353 | HCID 57894353 | 86.5% |
Reaction Steps
To a stirred EtOH (10 mL) solution containing N-toluenesulfonyl-2-(4-(trifluoroacetylaminomethyl)benzoyl)pyrrole (1.00 g, 2.20 mmol), was added 40% KOH solution (2 mL) and the mixture was heated at reflux until TLC analysis showed complete consumption of the starting material. The reaction mixture was then cooled to room temperature worked up as in Example 7. The crude product was suspended in H2O, filtered and dried to afford the purified product 2-(4-aminomethylbenzoyl)pyrrole (381 mg, 86%). 1H NMR (500 MHz, CD3OD, 25° C.) δ2.43 (s, 3H), 4.53 (s, 2H), 6.42 (m, 1H), 6.77 (m, 1H), 7.41 (d, 2H), 7.72 (d, 2H), 7.85 (m, 1H), 7.95 (d, 2H), 8.39 (t, 1H); 13C NMR (100 MHz, CD3OD, 25° C.) δ44.6, 109.7, 119.4, 125.6, 126.5, 128.4, 130.4, 136.8, 146.1, 184.6; HRMS (EI): m/z 200.0940 (100) {M}+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07691292B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-39f5aed54add4fc5853e193cf4f0cd47 |
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| Source note | uspto-grants-2010_04 |
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