HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → 3-(6-Methoxynaphthalen-2-yl)-9-methyl-3,9-diazaspiro[5.5]undecane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 3,9-Diazaspiro[5.5]undecane, 3-(6-methoxy-2-naphthalenyl)- | HCID 11984594 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | 3-(6-Methoxynaphthalen-2-yl)-9-methyl-3,9-diazaspiro[5.5]undecane | HCID 15940809 | 87.6% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To an ice cooled solution of 3-(6-methoxy-naphthalen-2-yl)-3,9-diaza-spiro[5.5]-undecane (294 mg, 0.95 mmol) in dichloroethane (20 mL), formaldehyde (37% in water, 204 μL, 2.84 mmol) was added and stirred for 1 h at 0° C. Sodium triacetoxyborohydride (402 mg, 1.89 mmol) was added and stirred at room temperature over night. The reaction was quenched with aqueous sodium hydrogencarbonate (sat.) and evaporated. The remaining aqueous phase was extracted three times with dichloromethane and the combined organic phase was dried (sodium sulfate), filtered and evaporated to give 270 mg (80%) of 3-(6-methoxy-naphthalen-2-yl)-9-methyl-3,9-diaza-spiro[5.5]undecane. Mp. 122.2-124.9° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07943630B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-58911322213c41249ed7ef5c398f4cd4 |
| Source note | uspto-grants-2011_05 |