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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1689221Generated: October 30, 2026

Borane;tetrahydrofuran → tert-Butyl 1-oxa-4,9-diazaspiro[5.5]undecane-9-carboxylate

https://huagongshe.com/reaction/1689221

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBorane;tetrahydrofuranHCID 2723981—
Reactant(Dimethyl sulfide)trihydroboronHCID 12423031—
Reactanttert-Butyl 3-oxo-1-oxa-4,9-diazaspiro[5.5]undecane-9-carboxylateHCID 57989097—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 1-oxa-4,9-diazaspiro[5.5]undecane-9-carboxylateHCID 53302318—

Reaction Steps

A solution of tert-butyl 3-oxo-1-oxa-4,9-diazaspiro[5.5]undecane-9-carboxylate (example 12, step a) (8.2 g) in THF (100 mL) was treated dropwise with borane THF complex (1M in THF, 91 mL) and the resultant mixture heated at 55° C. for 2 hours. Borane dimethylsulfide complex (2M in THF, 15.17 mL) was added and the resultant mixture heated at 55° C. for 2 hours. The mixture was cooled to room temperature and quenched with methanol, then the solvents were evaporated under reduced pressure. The residue was dissolved in methanol (250 mL) and the solution treated with N1,N2-dimethylethane-1,2-diamine (10 g) and the resultant mixture was heated at reflux for 6 hours. Further N1,N2-dimethylethane-1,2-diamine (3 g) was added and heated at reflux continued for 6 hours. The mixture was cooled to room temperature and the solvents evaporated under reduced pressure, the residue was purified by flash silica chromatography eluting with 1% triethylamine and 5% methanol in dichloromethane. Pure fractions were evaporated to dryness to afford the subtitled compound. Yield 7.40 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148373B2
Source datasetuspto-grants-2012_04
ORD IDord-3208326de15443a0adaeb9dc960928f1
Source noteuspto-grants-2012_04