HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1403207Generated: November 2, 2026
Acetonitrile → [(4-Bromo-2-methoxyphenyl)ethynyl](trimethyl)silane
https://huagongshe.com/reaction/1403207
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | 4-Bromo-1-iodo-2-methoxybenzene | HCID 46835731 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Product | [(4-Bromo-2-methoxyphenyl)ethynyl](trimethyl)silane | HCID 71239496 | 96.5% |
Reaction Steps
To a solution of 4-bromo-1-iodo-2-methoxybenzene (1.634 g, 5.221 mmol) in dry acetonitrile (20 mL) CuI (49.7 mg, 0.261 mmol) and Pd(Ph3P)2Cl2 (183.2 mg, 0.261 mmol) were added under Argon atmosphere and the mixture was degassed and backfilled with Argon for three times. TEA (0.728 mL, 5.221 mmol) and (ethynyl)trimethylsilane (1.48 mL, 1.03 g, 10.442 mmol) were added with a syringe and the reaction mixture, that darkened within 10 min, was stirred at room temperature for 1 h. The solvent was removed under vacuum and the residue was taken up with EtOAc (100 mL), washed with brine (3×20 mL), water (20 mL), dried over sodium sulphate and evaporated to dryness. The crude was purified by chromatography on silica gel (petroleum ether/diethyl ether 9/1) to yield the title compound as an orange solid (1.426 g, 96.5%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08912200B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-8a9eb1b6ae634907ad4dd40e4180d91b |
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| Source note | uspto-grants-2014_12 |
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