HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1963287Generated: October 29, 2026
Chlorotrimethylsilane → HCID 178506138, compound
https://huagongshe.com/reaction/1963287
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | Zinc | HCID 23994 | — |
| Reactant | 1-(Bromomethyl)-2-(trifluoromethyl)benzene | HCID 123057 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178506138 | HCID 178506138 | — |
Reaction Steps
In a dried flask zinc powder (2.489 g, 38.07 mmol) was suspended in anhydrous tetrahydrofuran (50 mL) under nitrogen. The resulting suspension was warmed to 60° C., then 1,2-dibromoethane (0.126 mL, 1.46 mmol) was added and stirred at that temperature for 15 min. It was cooled to room temperature, then chlorotrimethylsilane (0.149 mL, 1.17 mmol) was added and stirred for 20 min. 1-(Bromomethyl)-2-(trifluoromethyl)benzene (4.46 mL, 29.28 mmol) in THF (2 mL) was added dropwise and stirring was continued at room temperature for 4 h. Stirring was switched off to let the precipitates settle. The supernatant was used in the next transformation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08415378B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-7cef36f8b2214669a5527564a08fc9cf |
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| Source note | uspto-grants-2013_04 |
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