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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1188359Generated: November 2, 2026

Trimethylsilylacetylene → HCID 57800198, compound

https://huagongshe.com/reaction/1188359

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantHCID 57800179HCID 57800179—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418476HCID 178418476—
SolventTriethylamineHCID 8471—
ProductHCID 57800198HCID 57800198—

Reaction Conditions

Temperature50 °C

Reaction Steps

A triethylamine (2.2 mL) solution of N-[4-chloro-2-iodo-3-(trifluoromethyl)phenyl]-2,2-dimethylpropanamide (0.413 g, 1.02 mmol) was treated with TMS acetylene (0.158 mL, 1.12 mmol) followed by copper iodide (0.019 g, 0.102 mmol) and PdCl2(PPh3)2 (0.021 g, 0.031 mmol). The reaction vessel was purged with N2, sealed and heated to 50° C. for 14 h. TLC at this time showed excellent conversion to the desired product. The cooled mixture was filtered through a plug of celite and partitioned between EtOAc (10 mL) and H2O (10 mL). The organic portion was dried (Na2SO4), filtered, and concentrated. Column chromatography (SiO2, EtOAc/hexanes) afforded the title compound as a light brown solid: 1H NMR (CDCl3) δ 8.72 (bs, 1H), 8.64 (d, J=6.0 Hz, 1H), 7.41 (d, J=6.0 Hz, 1H), 1.34 (s, 9H), 0.29 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673948B2
Source datasetuspto-grants-2014_03
ORD IDord-b1612601a5b6434496023264550bec4b
Source noteuspto-grants-2014_03