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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 592341Generated: October 30, 2026

Water → Methyl 1-(2-ethynylphenyl)cyclopropanecarboxylate

https://huagongshe.com/reaction/592341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantMethyl 1-(2-((trimethylsilyl)ethynyl)phenyl)cyclopropanecarboxylateHCID 86712271—
SolventDichloromethaneHCID 6344—
ProductMethyl 1-(2-ethynylphenyl)cyclopropanecarboxylateHCID 86712270—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of methyl 1-(2-((trimethylsilyl)ethynyl)phenyl)cyclopropanecarboxylate (I5) (568 mg, 2.09 mmol) in DCM (20.0 mL) at 0° C. was added TBAF (1.0 M in THF, 3.13 mL, 3.13 mmol). The resulting mixture was stirred at 0° C. for 10 minutes then poured into water (50 mL). The aqueous layer was extracted with DCM (2×50 mL), then the combined organic layers were washed with brine, dried over MgSO4 and the solvent was removed in vacuo. The residue was adsorbed onto silica gel and purified by column chromatography (Biotage Isolera, SiO2 cartridge, 0-25% EtOAc in petroleum benzine 40-60° C.) to give the title compound K2 as an off-white solid (140 mg, 34%); 1H NMR (400 MHz, d6-DMSO) δ 7.46 (dt, J=7.5, 0.8 Hz, 1H), 7.40-7.25 (m, 3H), 4.32 (s, 1H), 3.52 (s, 3H), 1.54 (q, J=4.1 Hz, 2H), 1.25-1.19 (m, 2H). LCMS-A: rt 5.921 min; m/z 201 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238644B2
Source datasetuspto-grants-2016_01
ORD IDord-21542976f9c44273810d60b4a75c6f3f
Source noteuspto-grants-2016_01