HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 439932Generated: October 30, 2026
Ethyl 6-(3-tert-butylphenylethynyl)nicotinate → 6-(3-Tert-butylphenylethynyl)nicotinic acid
https://huagongshe.com/reaction/439932
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl 6-(3-tert-butylphenylethynyl)nicotinate | HCID 14989669 | — |
| Solvent | Potassium Hydroxide | HCID 14797 | — |
| Product | 6-(3-Tert-butylphenylethynyl)nicotinic acid | HCID 14989672 | — |
Reaction Steps
A solution of 60 mg (0.195 mmol) of ethyl 6-(3-tert-butylphenylethynyl)nicotinate (Compound 1) in 4 ml of aqueous ethanolic KOH was stirred at room temperature for 24 hours. The mixture was concentrated in-vacuo and the residue was treated with 5 ml of water and 5 ml of ether. The aqueous layer was separated and washed with a further 5 ml of ether. The aqueous layer was then acidified with 3 ml of 10 percent HCl and extracted with 2×5 ml of ether. The ether extracts were combined and washed with saturated NaCl solution and then dried (MgSO4). The solution was concentrated in-vacuo to give the title compound as a pale yellow solid. PMR (CDCl3): & 1.26 (9H, s), 7.25 (1H, t, J-7.8 Hz), 7.35-7.42 (2H, m), 7.56-7.63 (2H, m), 8.35 (1H, dd, J-8.2 H, 2.1 Hz), 9.31 (1H, d, J-2.1 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05516904 |
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| Source dataset | uspto-grants-1996_05 |
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| ORD ID | ord-1e1da2974cb44810b0d39989f43bcb16 |
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| Source note | uspto-grants-1996_05 |
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