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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1861493Generated: November 2, 2026

Trimethylsilylacetylene → HCID 131722720, compound

https://huagongshe.com/reaction/1861493

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantHCID 131722721HCID 131722721—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductHCID 131722720HCID 13172272078%

Reaction Conditions

Temperature95 °C

Reaction Steps

To a solution of 4-(tert-butyl-dimethyl-silanyloxymethyl)-3-isopropyl-phenyl 1,1,1-trifluoro-methansulfonate (Intermediate 150, 970.0 mg, 2.35 mmols) in triethylamine (2 mL) and 6 mL DMF was sparged with argon for 15 minutes. Trimethylsilyl acetylene (1.00 g, 10.6 mmols) was then added followed by dichlorobis(triphenylphosphine)palladium(II) (66.0 mg, 0.09 mmol). The resulting reaction mixture was heated to 95° C. for 20 hours. The solution was cooled to room temperature and concentrated under reduced pressure. The title compound (200.0 mg, 78%) was isolated by chromatography (0-25% EtOAc-hexanes) as an orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06531599B2
Source datasetuspto-grants-2003_03
ORD IDord-0367a06167de4269b59bda5808b4121b
Source noteuspto-grants-2003_03