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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748940Generated: November 1, 2026

Trimethylsilylacetylene → HCID 86719903, compound

https://huagongshe.com/reaction/1748940

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantHCID 86719904HCID 86719904—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventDiisopropylamineHCID 7912—
ProductHCID 86719903HCID 8671990353.5%

Reaction Steps

Trimethylsilylacetylene (3.1 mL, 21.43 mmol), PdCl2(PPh3)2 (400 mg, 0.6 mmol), and CuI (235 mg, 0.79 mmol) were added successively to a deaerated solution of 2,5-dibromo-3,6-dichloro-1,4-diethylhexyloxybenzene (10) (4.00 g, 7.14 mmol) in diisopropylamine (25 mL) and toluene (55 mL). The resulting mixture was refluxed for 48 hours, then diluted with water (150 mL), and extracted with hexane (2×80 mL). The extract was washed with water (2×80 mL) and dried (MgSO4). Evaporation of the solvent gave an oily residue, which was purified by column chromatography (hexane:CH2Cl2, 98:2) to give an orange-red solid (1.90 gm, 45%). 1H-NMR(CDCl3): δ 3.87 (m, 4H), 1.81 (m, 2H), 1.31-1.64 (m, 12H), 0.97 (t, J=7.5 Hz, 6H), 0.92 (t, J=7.5 Hz, 6H). MS (EI): Calculated. 595.8. found [M+I]+, 596.8.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09153785B2
Source datasetuspto-grants-2015_10
ORD IDord-48ad068792474f268e5797ee3bdd112c
Source noteuspto-grants-2015_10