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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 335258Generated: October 29, 2026

Chlorotrimethylsilane → Tert-butyl 4-(2-(trimethylsilyloxy)allyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/335258

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantSodium BicarbonateHCID 516892—
ReactantLithium diisopropylamideHCID 2724682—
ReactantTert-butyl 4-(2-oxopropyl)piperidine-1-carboxylateHCID 12017169—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 4-(2-(trimethylsilyloxy)allyl)piperidine-1-carboxylateHCID 66994845108.1%

Reaction Steps

To a cooled (−78° C.) solution of LDA (12.3 mL, 24.6 mmol) in THF (50 mL) was added dropwise over 40 minutes a solution of tert-butyl 4-(2-oxopropyl)piperidine-1-carboxylate (4.95 g, 20.5 mmol) in THF (20 mL). After an additional 25 minutes, chlorotrimethylsilane (5.21 mL, 41.0 mmol) was added dropwise over 20 minutes. After stirring for an hour, the reaction was poured into saturated NaHCO3 and extracted with ether (2×400 mL). The combined ether layers were washed with brine, dried, filtered and concentrated to afford the title compound (6.95 g, 108% yield) which was used as is in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883828B2
Source datasetuspto-grants-2014_11
ORD IDord-bf909ac08ead4168b866905341c6efb3
Source noteuspto-grants-2014_11