HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1690049Generated: October 30, 2026
Sulfuric Acid → 5-Trifluoromethyl-1H-pyrrolo[2,3-b]pyridine 2-ethyl carboxylate
https://huagongshe.com/reaction/1690049
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 5-(trifluoromethyl)-1H-pyrrolo(2,3-b)pyridine-2-carboxylic acid | HCID 54758843 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-Trifluoromethyl-1H-pyrrolo[2,3-b]pyridine 2-ethyl carboxylate | HCID 86639056 | 172.3% |
Reaction Steps
Put 0.3 g (1.3 mmol) of 5-trifluoromethyl-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid (Angew Chem Int Ed 2004, 43(34), 4526-4528) and 50 mL of ethanol in a 100-mL flask equipped with a magnetic stirrer. Add, to this solution, 0.5 mL of concentrated sulfuric acid. The reaction mixture is then refluxed for 18 hours. The cooled solution is concentrated to dryness at reduced pressure. The residue is taken up in dichloromethane (100 mL), the organic phase is washed successively with a normal aqueous solution of sodium hydroxide (30 mL), with water (20 mL) and then with a saturated aqueous solution of sodium chloride. It is dried over sodium sulfate and then concentrated at reduced pressure. 0.29 g (1.12 mmol) of the expected product is isolated in the form of a yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08153650B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-30bd407b0d95495f861febee0eba25ad |
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| Source note | uspto-grants-2012_04 |
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