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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1964242Generated: October 31, 2026

Trimethylsilylacetylene → Methyl 1-(4-amino-3-((trimethylsilyl)ethynyl)phenyl)cyclopropanecarboxylate

https://huagongshe.com/reaction/1964242

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantMethyl 1-(4-amino-3-bromophenyl)cyclopropanecarboxylateHCID 59129194—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
CatalystHCID 178418476HCID 178418476—
SolventTriethylamineHCID 8471—
ProductMethyl 1-(4-amino-3-((trimethylsilyl)ethynyl)phenyl)cyclopropanecarboxylateHCID 5912946756%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a degassed solution of methyl 1-(4-amino-3-bromophenyl)cyclopropane carboxylate (8 g, 0.03 mol) in Et3N (100 mL) was added ethynyl-trimethyl-silane (30 g, 0.3 mol), DMAP (5% mol) and Pd(PPh3)2Cl2 (5% mol) under N2. The mixture was refluxed at 70° C. overnight. The insoluble solid was filtered off and washed with EtOAc (100 mL×3). The filtrate was evaporated under reduced pressure to give a residue, which was purified by chromatography column on silica gel (petroleum ether/ethyl acetate=20:1) to give methyl 1-(4-amino-3-((trimethylsilyl)ethynyl)phenyl)cyclopropanecarboxylate (4.8 g, 56%). 1H NMR (300 MHz, CDCl3) δ7.27 (s, 1 H), 7.10 (dd, J=2.1, 8.4 Hz, 1 H), 6.64 (d, J=8.4 Hz, 1 H), 3.60 (s, 3 H), 1.55-1.51 (m, 2 H), 1.12-1.09 (m, 2 H), 0.24 (s, 9 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415387B2
Source datasetuspto-grants-2013_04
ORD IDord-9943bfea93564ef88bb682ff93b99091
Source noteuspto-grants-2013_04