Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2272398Generated: November 2, 2026

Trimethylsilylacetylene → Methyl 2-(2-((trimethylsilyl)ethynyl)phenyl)acetate

https://huagongshe.com/reaction/2272398

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantMethyl 2-(2-iodophenyl)acetateHCID 640185—
CatalystHCID 178418476HCID 178418476—
ProductMethyl 2-(2-((trimethylsilyl)ethynyl)phenyl)acetateHCID 59457733—

Reaction Steps

Methyl 2-(2-iodophenyl)acetate (I9) (4.65 g, 16.8 mmol), PdCl2(PPh3)2 (295 mg, 421 μmol) and Cu(I)I (80.0 mg, 421 μμmol) were placed into an oven dried reaction flask under nitrogen. (Trimethylsilyl)acetylene (2.80 mL, 20:2 mmol), dry degassed THF (20 mL) and triethylamine (20 mL) were added and the reaction mixture was stirred at room temperature for 16 hours. The volatiles were removed under reduced pressure to give a black residue which was adsorbed onto silica then chromatographed on silica gel (0-5% ethyl acetate/petroleum benzine 40-60° C.) to give the title compound (I10) (4.63 g, 99%) as a light brown liquid; 1H NMR (400 MHz, CDCl3) δ 7.48 (dd, J=7.5, 0.8 Hz, 1H), 7.32-7.14 (m, 3H), 3.84 (s, 2H), 3.71 (s, 3H), 0.26 (s, 9H). LCMS Method C: rt 6.64 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120761B2
Source datasetuspto-grants-2015_09
ORD IDord-0480d1ff194b4aacaf818983a11b6db8
Source noteuspto-grants-2015_09