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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 852684Generated: October 30, 2026

Triphenylphosphine → Tert-butyl 2-oxa-8-azaspiro[4.5]decane-8-carboxylate

https://huagongshe.com/reaction/852684

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactanttert-Butyl 4-(2-hydroxyethyl)-4-(hydroxymethyl)piperidine-1-carboxylateHCID 21955304—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 2-oxa-8-azaspiro[4.5]decane-8-carboxylateHCID 2195522765%

Reaction Conditions

Temperature0 °C

Reaction Steps

Diethyl azodicarboxylate (183 μl, 1.16 mmol) in tetrahydrofuran (0.5 mL) was added dropwise to a stirred, cooled (0° C.) solution of 1,1-dimethylethyl 4-(2-hydroxyethyl)-4-(hydroxymethyl)-1-piperidinecarboxylate Description 24, 250 mg, 0.96 mmol) and triphenylphosphine (303 mg, 1.16 mmol) in tetrahydrofuran (10 mL) and the mixture was stirred at 0° C. for 90 minutes then at room temperature overnight. The mixture was cooled to 0° C. and further triphenylphosphine (126 mg, 0.48 mmol) and diethyl azodicarboxylate (76 μl, 0.48 mmol) were added. The mixture was stirred at room temperature for 2.5 hours, then the solvent was evaporated under reduced pressure and the residue was purified by flash column chromatography on silica gel, eluting with isohexane/EtOAc (80:20), to give the title compound as a colorless oil (150 mg, 65%). m/z (ES+) 186 (M+1−C4H8).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253205B2
Source datasetuspto-grants-2007_08
ORD IDord-01a3a0d0f48845b78e6ea94a3409b585
Source noteuspto-grants-2007_08