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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1782023Generated: October 30, 2026

Water → tert-Butyl 1-oxa-6-azaspiro(2.5)octane-6-carboxylate

https://huagongshe.com/reaction/1782023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSulfoxonium, trimethyl-, iodide (1:1)HCID 74498—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
ReactantPotassium tert-butoxideHCID 23665647—
Solvent1,2-DimethoxyethaneHCID 8071—
Producttert-Butyl 1-oxa-6-azaspiro(2.5)octane-6-carboxylateHCID 2213556481%

Reaction Steps

Potassium t-butoxide (31 g) was added to a stirred suspension of trimethylsulfoxonium iodide (60.8 g) in 1,2-dimethoxyethane (250 ml) at 20° C. After 1 hour, the mixture was added portionwise over 30 minutes to a stirred solution of 4-oxo-1-piperidinecarboxylic acid, 1,1-dimethylethyl ester (50 g) in 1,2-dimethoxyethane (50 ml) at 0° C. After a further 2 hours, water (500 ml) was added and the mixture extracted with tert.-butyl methyl ether (2×500 ml). The organic extracts were washed separately with saturated sodium bicarbonate solution (250 ml), combined, dried over anhydrous magnesium sulphate, filtered and evaporated under reduced pressure. The residual oil was co-evaoprated with toluene (100 ml) to give the sub-title compound (43.25 g, 81%) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07498338B2
Source datasetuspto-grants-2009_03
ORD IDord-62c7a6143c584a9fa367b7bf3a5fe3c7
Source noteuspto-grants-2009_03