HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53171Generated: October 29, 2026
Chlorotrimethylsilane → HCID 15379438, compound
https://huagongshe.com/reaction/53171
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | 6-Bromo-3-methyl[1,3]oxazolo[4,5-b]pyridin-2(3H)-one | HCID 15926016 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 15379438 | HCID 15379438 | — |
Reaction Steps
Zinc (227 mg, 3.48 mmol) is suspended in tetrahydrofuran (10 ml) and 1,2-dibromoethane (0.22 ml, 0.2 mmol) is added. The mixture is heated at 60° C. for 3 minutes, the solution is allowed to cool until the temperature is 35° C., and trimethylsilyl chloride (0.06 ml, 0.5 mmol) is slowly added. Stirring is maintained for 30 minutes and then benzyl bromide (0.11 ml, 0.9 mmol) is added. Wait a further 30 minutes before introducing 6-bromo-3-methyloxazolo[4,5-b]pyridin-2(3H)-one (200 mg, 0.87 mmol) and tetrakis(triphenylphosphine)palladium (4 mg). Heat at 50° C. for 20 minutes. After the solution has been cooled, the zinc is removed by filtration, the flitrate is taken up in water, and then a 10% aqueous hydrochloric acid solution is added until the aqueous phase becomes clear. Extraction is carried out with dichloromethane. The organic phase is dried over magnesium sulfate and filtered, and then the solvent is evaporated off under reduced pressure. The title product is purified by chromatography on silica gel (eluant: dichloromethane). The yield obtained is 91%. ##STR51##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05618819 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-b4a73ef744a14bab9fa46296894a21b5 |
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| Source note | uspto-grants-1997_04 |
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