HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 324005Generated: October 28, 2026
Chlorotrimethylsilane → HCID 13227592, compound
https://huagongshe.com/reaction/324005
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Ethyl cyclopropaneacetate | HCID 12453023 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 13227592 | HCID 13227592 | — |
Reaction Steps
A solution of n-butyllithium in hexanes (1.6M, 26 ml) was added with stirring to a solution of diisopropylamine (6.2 ml) in tetrahydrofuran (8 ml) at below −25° C. under nitrogen. After 30 min, the mixture was cooled to −75° C. and ethyl cyclopropylacetate (4.5 g) added dropwise keeping the temperature below −65° C. The mixture was then maintained below −75° C. for 3 h before chlorotrimethylsilane (3.8 ml) was added below −65° C. The reaction was allowed to warm to ambient temperature and then evaporated to dryness. The residue was slurried with hexane and filtered. The filtrate was evaporated to an orange oil which was distilled in vacuo to give the title compound (4.0 g) as a clear mobile liquid, b.p 80-82° C., 3×10−2 bar.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06215002B1 |
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| Source dataset | uspto-grants-2001_04 |
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| ORD ID | ord-7e4ac2840dfa464191ce82b86dbf27bb |
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| Source note | uspto-grants-2001_04 |
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