HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1963335Generated: October 30, 2026
Chlorotrimethylsilane → HCID 178505823, compound
https://huagongshe.com/reaction/1963335
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | Zinc | HCID 23994 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | 3,4,5-Trifluorobenzyl bromide | HCID 2777062 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178505823 | HCID 178505823 | — |
Reaction Steps
Zinc powder (2.62 g, 40.00 mmol) and lithium chloride (1.696 g, 40.00 mmol) were added to a dried flask and heated to 150° C. under vacuum for 30 min. The flask was allowed to reach room temperature. THF (20 mL) and 1,2-dibromoethane (0.115 mL, 1.33 mmol) were added. The mixture was heated until boiling occurred and the flask was then allowed to reach room temperature. Chlorotrimethylsilane (0.034 mL, 0.27 mmol) was added and the mixture was again heated until boiling occurred. The flask was cooled with an ice-bath and 5-(bromomethyl)-1,2,3-trifluorobenzene (6 g, 26.67 mmol) dissolved in THF (5 mL) was then added dropwise. The ice-bath was removed and the reaction stirred at room temperature for 20 h. Solids were allowed to settle and the supernatant 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-d8fa14aa9e404e519b83680924685a75 |
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| Source note | uspto-grants-2013_04 |
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