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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 592352Generated: October 30, 2026

Acetic Acid → 1-(2-Ethynylphenyl)cyclopropanecarboxamide

https://huagongshe.com/reaction/592352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantTetrahydrofuranHCID 8028—
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant1-(2-((Trimethylsilyl)ethynyl)phenyl)cyclopropanecarboxamideHCID 86712275—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product1-(2-Ethynylphenyl)cyclopropanecarboxamideHCID 8671227699.6%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238644B2
Source datasetuspto-grants-2016_01
ORD IDord-de8e3fa5a8f8411b8247d5c6be0f8118
Source noteuspto-grants-2016_01