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
Participants
| Role | Name | HCID | Charge |
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| Reactant | (Dimethyl sulfide)trihydroboron | HCID 12423031 | — |
| Reactant | Tert-butyl 9-oxo-7-oxa-3,10-diazaspiro[5.6]dodecane-3-carboxylate | HCID 57989131 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tert-butyl 7-oxa-3,10-diazaspiro[5.6]dodecane-3-carboxylate | HCID 57989265 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08148373B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-906c4ee88dff4c698a914841aeb9765d |
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| Source note | uspto-grants-2012_04 |
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