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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 514800Generated: October 30, 2026

Sulfoxonium, trimethyl-, iodide (1:1) → tert-Butyl 1-oxa-6-azaspiro(2.5)octane-6-carboxylate

https://huagongshe.com/reaction/514800

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfoxonium, trimethyl-, iodide (1:1)HCID 74498—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
ReactantPotassium tert-butoxideHCID 23665647—
Solvent1-ButanolHCID 263—
Producttert-Butyl 1-oxa-6-azaspiro(2.5)octane-6-carboxylateHCID 22135564—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of tert-butyl 4-oxopiperidine-1-carboxylate (5 g, 25 mmol) in BuOH (20 mL) was added potassium tert-butoxide (4.125 g, 18.75 mmol). The mixture was stirred at 50° C. for 1 h. Then trimethyl sulfoxonium iodide (11 g, 50 mmol) was added to the mixture, and the resulting reaction mixture was stirred at 50° C. overnight. When TLC showed that s.m. was consumed, the mixture was cooled and filtered. The filtrate was concentrated to give the crude product which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108921B2
Source datasetuspto-grants-2015_08
ORD IDord-cafb405adf1a4336b65848cc31a42db2
Source noteuspto-grants-2015_08