Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1689440Generated: October 25, 2026

(Dimethyl sulfide)trihydroboron → Tert-butyl 7-oxa-3,10-diazaspiro[5.6]dodecane-3-carboxylate

https://huagongshe.com/reaction/1689440

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Dimethyl sulfide)trihydroboronHCID 12423031—
ReactantTert-butyl 9-oxo-7-oxa-3,10-diazaspiro[5.6]dodecane-3-carboxylateHCID 57989131—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 7-oxa-3,10-diazaspiro[5.6]dodecane-3-carboxylateHCID 57989265—

Reaction Conditions

Temperature70 °C

Reaction Steps

Borane-methyl sulfide complex (2M in THF, 2.88 mL) was added to a solution of tert-butyl 9-oxo-7-oxa-3,10-diazaspiro[5.6]dodecane-3-carboxylate (example 89, step d) (0.41 g) in dry THF (40 mL) and the reaction mixture then heated at 70° C. for 30 minutes under nitrogen. The mixture was cooled to room temperature and quenched with methanol. The solvents were removed under reduced pressure and the residue dissolved in methanol (100 mL). N1,N2-dimethylethane-1,2-diamine (1.0 g) was added and the mixture heated at reflux under nitrogen for 16 h. Further N1,N2-dimethylethane-1,2-diamine (1.0 g) was added and refluxing continued for 16 h. The solvents were evaporated under reduced pressure and the residue azeotroped with toluene. The crude product was purified by flash silica chromatography using 6% methanol in dichloromethane with 1% triethylamine as solvent. Pure fractions were evaporated to dryness to afford the subtitled compound. Yield 0.176 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148373B2
Source datasetuspto-grants-2012_04
ORD IDord-906c4ee88dff4c698a914841aeb9765d
Source noteuspto-grants-2012_04