Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378503Generated: October 26, 2026

Chlorotrimethylsilane → ethyl N-trimethylsilylpiperidin-4-ylcarboxylate

https://huagongshe.com/reaction/378503

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTriethylamineHCID 8471—
ReactantEthyl 4-piperidinecarboxylateHCID 70770—
SolventDiethyl EtherHCID 3283—
Productethyl N-trimethylsilylpiperidin-4-ylcarboxylateHCID 2200694579%

Reaction Steps

Under a nitrogen atmosphere, a stirred solution of 100.0 grams (0.64 mole) of ethyl piperidin-4-ylcarboxylate and 94 mL (0.67 mole) of triethylamine in 1400 mL of diethyl ether was cooled to 15° C., and a solution of 86 mL (0.68 mole) of chlorotrimethylsilane in 100 mL of diethyl ether was added dropwise during a 30 minute period. Upon completion of the addition, the thick reaction mixture was stirred vigorously for one hour while warming to ambient temperature. The reaction mixture was then filtered, and the collected solid was washed with diethyl ether. The combined wash and filtrate were concentrated under reduced pressure to a residual oil. The oil was distilled under reduced pressure, yielding 115.0 grams (79% yield) of ethyl N-(trimethylsilyl)piperidin-4-ylcarboxylate, bp 75° C./0.1 mm Hg. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06030987
Source datasetuspto-grants-2000_02
ORD IDord-fc9f0162328a4f968ee605aa83ee8d79
Source noteuspto-grants-2000_02