HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 86642466, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3,3-Difluoroazetidine hydrochloride | HCID 2758247 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | tert-Butyl 9-oxo-3-azaspiro[5.5]undecane-3-carboxylate | HCID 51072194 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 86642466 | HCID 86642466 | — |
Reaction Steps
tert-Butyl 9-oxo-3-azaspiro[5.5]undecane-3-carboxylate (for the synthesis, see above) (1 g, 3.74 mmol) was added to 3,3-difluoroazetidine hydrochloride (0.484 g, 3.74 mmol) and triethylamine (0.52 ml, 3.74 mmol) in 1,2-dichloroethane (15 ml). The mixture was stirred for 5 min and sodium triacetoxyborohydride (1.1 g, 5.23 mmol) was subsequently added and the mixture was stirred at room temperature for 3 d. Saturated sodium bicarbonate solution was added and after separation of the phases the aqueous phase was extracted with methylene chloride (2×). The combined organic phases were washed with saturated sodium chloride solution (1×), dried over magnesium sulfate and concentrated in vacuo. Yield: 1.26 g (98%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08119805B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-9fd63c8e3e734d5fa6338d7be56de6ac |
| Source note | uspto-grants-2012_02 |