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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1804596Generated: October 26, 2026

Chlorotrimethylsilane → Tert-butyl 4-{1-[(trimethylsilyl)oxy]vinyl}piperidine-1-carboxylate

https://huagongshe.com/reaction/1804596

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantLithium diisopropylamideHCID 2724682—
Reactant4-Acetyl-piperidine-1-carboxylic acid tert-butyl esterHCID 10987983—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 4-{1-[(trimethylsilyl)oxy]vinyl}piperidine-1-carboxylateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354403B2
Source datasetuspto-grants-2013_01
ORD IDord-586d6020c288419283ad23b235d63148
Source noteuspto-grants-2013_01