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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2303616Generated: November 2, 2026

Potassium bis(trimethylsilyl)amide → tert-Butyl 4-(prop-2-en-1-yl)piperidine-1-carboxylate

https://huagongshe.com/reaction/2303616

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
Reactanttert-Butyl 4-(2-oxoethyl)piperidine-1-carboxylateHCID 10353694—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Producttert-Butyl 4-(prop-2-en-1-yl)piperidine-1-carboxylateHCID 1111772272.2%

Reaction Steps

A solution of methyltriphenylphosphonium bromide (5.3 g, 14.8 mmol) in TBF (50 mL) was cooled to 0° C. under nitrogen. Potassium hexamethyl disilazide (27.7 mL, 0.5M toluene solution, 13.9 mmol) was added and the mixture was stirred for 30 min. A solution of (1-t-butoxycarbonylpiperidin-4-yl)acetaldehyde from Step A (2.25 g, 9.9 mmol) in THF (10 mL) was added and the mixture was warmed to rt. After 30 min, the reaction was complete by tlc analysis. The mixture was diluted with ethyl acetate (200 mL) and washed with water and brine (100 mL each). The organic phase was dried over sodium sulfate and concentrated to give an oil which was purified by FC (75 g silica, 10/1 hexane/ethyl acetate) to afford the title compound (1.61 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06432981B1
Source datasetuspto-grants-2002_08
ORD IDord-655ba462856749b4bcacbd30c87977a6
Source noteuspto-grants-2002_08