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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 634853Generated: October 25, 2026

Chlorotrimethylsilane → ethyl N-trimethylsilylpiperidin-4-ylcarboxylate

https://huagongshe.com/reaction/634853

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 numberUS06184234B2
Source datasetuspto-grants-2001_02
ORD IDord-7da67381cc7b4c3f98f5c17c0e82f623
Source noteuspto-grants-2001_02