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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1590945Generated: October 25, 2026

Tributylstannane → 4-Benzoyloxy-1-t-butoxy-2,2,6,6-tetramethylpiperidine

https://huagongshe.com/reaction/1590945

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylstannaneHCID 5948—
Reactant2-Iodo-2-methylpropaneHCID 11206—
Reactant1-Hydroxy-4-benzoyloxy-2,2,6,6-tetramethylpiperidineHCID 688178—
SolventChlorobenzeneHCID 7964—
Product4-Benzoyloxy-1-t-butoxy-2,2,6,6-tetramethylpiperidineHCID 1299690744.5%

Reaction Steps

A solution of 56.0 g (203 mmol) of 4-benzoyloxy-1-oxyl-2,2,6,6-tetramethylpiperidine, 125 ml of chlorobenzene, and 58.9 g of t-butyl iodide is cooled to 5° C. Tri-n-butyltin hydride (29 g, 100 mmol) is added dropwise over 110 minutes while the temperature is maintained below 20° C. The reaction mixture is concentrated at reduced pressure and then purified by silica gel chromatography (200:1, then 100:3 heptane:ethyl acetate) to afford 30.1 g of a white solid, m.p. 80°-82.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05204473
Source datasetuspto-grants-1993_04
ORD IDord-03b8a0f652b34942ad38273eb81f18a7
Source noteuspto-grants-1993_04