HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 592352Generated: October 30, 2026
Acetic Acid → 1-(2-Ethynylphenyl)cyclopropanecarboxamide
https://huagongshe.com/reaction/592352
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | 1-(2-((Trimethylsilyl)ethynyl)phenyl)cyclopropanecarboxamide | HCID 86712275 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(2-Ethynylphenyl)cyclopropanecarboxamide | HCID 86712276 | 99.6% |
Reaction Steps
A cooled (5° C. water/ice bath) solution of 1-(2-((trimethylsilyl)ethynyl)phenyl)cyclopropanecarboxamide (I12) (1.09 g, 4.23 mmol) in DCM (20 mL) containing acetic acid (0.315 mL, 5.50 mmol) was slowly treated with a 1 M solution of TBAF in THF (5.08 mL, 5.08 mmol). The resulting mixture was stirred at room temperature for 2 hours then water (30 mL) was added. The aqueous layer was extracted with DCM (2×15 mL), then the combined organic extracts were washed with water, brine, dried (MgSO4), filtered and evaporated in vacuo to give the title compound as a tan solid (0.780 g, 99%); 1H NMR (300 MHz, CDCl3) δ 7.57 (d, J=6.7 Hz, 1H), 7.31-7.45 (m, 3H), 5.46 (brs, 1H), 5.27 (brs, 1H), 3.38 (s, 1H), 1.75 (dq, J=4.0 Hz, 2H) 1.18 (dq, J=3.7 Hz, 2H). LCMS-B: rt 5.489 min; m/z 186 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09238644B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-de8e3fa5a8f8411b8247d5c6be0f8118 |
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| Source note | uspto-grants-2016_01 |
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