HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Bicarbonate → Tert-butyl 2-hydroxy-7-azaspiro[3.5]nonane-7-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Tert-butyl 2-oxo-7-azaspiro[3.5]nonane-7-carboxylate | HCID 11195798 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Tert-butyl 2-hydroxy-7-azaspiro[3.5]nonane-7-carboxylate | HCID 9834677 | 57% |
Reaction Steps
To a solution of tert-butyl 2-oxo-7-azaspiro[3.5]nonane-7-carboxylate (600 mg, 2.5 mmol, 1.0 equiv) in MeOH (6.0 mL) was added sodium borohydride (190 mg, 5.0 mmol, 2.0 equiv) in portions at 0° C. under nitrogen. The mixture was stirred at room temperature for 2.0 hrs. The solution was concentrated by evaporator to give the white solid. Saturated NaHCO3 solution (40 mL) was added. The aqueous phase was extracted with DCM (4×30 mL). The combined organic phase was dried over anhydrous Na2SO4, concentrated to give the crude which was purified by CombiFlash (24 g silica gel column, EtOAc/Hexane=0-60%) to afford 334 mg (yield 57%) of tert-butyl 2-hydroxy-7-azaspiro[3.5]nonane-7-carboxylate as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09226923B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-f8c888775fca44afa279ba566c711b7b |
| Source note | uspto-grants-2016_01 |