HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Sulfoxide → 5-Benzyl-1-oxa-5-azaspiro[2.5]octane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-Piperidinone, 1-(phenylmethyl)- | HCID 96650 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Benzyl-1-oxa-5-azaspiro[2.5]octane | HCID 13720766 | 71% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
Sodium hydride (583 mg, 14.6 mmol) in DMSO (6 mL) was heated to 55° C. for 1 h. The reaction mixture is cooled to 0° C. and Me3SI (3 g, 14.62 mmol) dissolved in THF (9.8 mL) was added dropwise. 1-Benzyl-piperidine-3-one (1.5 g, 6.64 mmol) dissolved in DMSO (10 mL) was added 15 minutes later. After completion of addition the reaction proceded at RT. After 30 min. the reaction was quenched with water. The aqueous layer was extracted with hexanes. Combined organic layers were dried over Na2SO4 and concentrated. The crude material was purified using silica gel chromatography (9:1 DCM:hexanes in 2 M ammonia in EtOH) to yield 5-benzyl-1-oxa-5-aza-spiro[2.5]octane (960 mg, 71%). MH+ (204).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07132551B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-af85d8f5f543434eb12d0ff8dc255dae |
| Source note | uspto-grants-2006_11 |