HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081396Generated: November 1, 2026
Chlorotrimethylsilane → HCID 14774099, compound
https://huagongshe.com/reaction/1081396
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | 4,4-Dimethyl-2-(2,4,5-trifluorophenyl)-4,5-dihydro-1,3-oxazole | HCID 11009734 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 14774099 | HCID 14774099 | 83.1% |
Reaction Steps
A solution of 8.7 mL (62.1 mmol) of diisopropylamine in 100 mL of dry THF under argon was cooled to -78° C. and treated with 28.3 mL (56.6 mmol) of 2.0M n-butyllithium. The LDA solution was stirred at -78° C. for 15 minutes. To this solution was added a solution of 11.8 g (51.5 mmol) of 2-(2,4,5-trifluorophenyl)-4,4-dimethyl-2-oxazoline in 50 mL of THF, and the reaction mixture was stirred for 1 hour at -78° C. To the reaction mixture was added 13 mL (102.5 mmol) of chlorotrimethylsilane, and the solution was warmed to room temperature. Water was added; the organic layer was dried over magnesium sulfate and concentrated. The crude product was chromatographed on silica gel (E. Merck 230-400 Mesh), eluting with 80:20 chloroform:ethyl acetate to give 12.9 g of the title compound, mp 71°-72° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05585491 |
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| Source dataset | uspto-grants-1996_12 |
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| ORD ID | ord-f5d89336c91343ce97d9c2e867313943 |
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| Source note | uspto-grants-1996_12 |
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