HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorotrimethylsilane → Tert-butyl 4-{1-[(trimethylsilyl)oxy]vinyl}piperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | 4-Acetyl-piperidine-1-carboxylic acid tert-butyl ester | HCID 10987983 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tert-butyl 4-{1-[(trimethylsilyl)oxy]vinyl}piperidine-1-carboxylate | HCID 67972300 | — |
Reaction Steps
To a solution of LDA in THF (70 mL) under nitrogen atmosphere, cooled to −78° C. via dry ice/acetone bath, was added tert-butyl 4-acetylpiperidine-1-carboxylate (5 g, 22 mmol) in THF (30 mL) dropwise over 30 min. The resulting mixture was stirred for an additional 30 min and then TMSCl (2.81 mL) was added via syringe dropwise over 10 min and the resulting solution stirred for 1 h at −78° C. Quench with saturated sodium bicarbonate (300 mL) and extracted with ether (2×200 mL). Combined the organics, wash with brine, dry over sodium sulfate, filter, and concentrate under vacuum. The compound obtained (6.0 g, 92%) was used for the next reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08354403B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-586d6020c288419283ad23b235d63148 |
| Source note | uspto-grants-2013_01 |