HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356372Generated: October 29, 2026
Chlorotrimethylsilane → HCID 18630022, compound
https://huagongshe.com/reaction/356372
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Reactant | Cyclohexane | HCID 8078 | — |
| Reactant | HCID 4609051 | HCID 4609051 | — |
| Reactant | CID 53628100 | HCID 178418400 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18630022 | HCID 18630022 | 45% |
Reaction Steps
A solution of 1.3M s-BuLi in cyclohexane (23.91 mL, 31.1 mmol) was added to an ether/liquid N2 cooled (-90° C.) solution of TMEDA (3.97 g, 34.2 mmol) in THF (40 mL), followed by the addition of a solution of N-(3-fluorobenzoyl)pyrrolidine (5.0 g, 25.9 mmol) in a minimum volume of THF. The resulting reaction mixture was stirred at -90° C. for 15 min, then TMSCl (6.75 g, 62.2 mmol) was added in a single portion. The reaction was warmed to RT, quenched with dilute aq citric acid, then was extracted with ether (3X). The combined ether extracts were dried (MgSO4), concentrated, and purified by HPLC with 3:7 EtOAc/hexanes to afford 0.45 g of the title compound as an oil, a 45% yield, which solidified on standing to a white solid. m.p. 97°-100° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05834447 |
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| Source dataset | uspto-grants-1998_11 |
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| ORD ID | ord-a221860d3a8c49a99d008d215e82d3a4 |
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| Source note | uspto-grants-1998_11 |
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