HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium triacetoxyborohydride → HCID 67025565, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | rel-(2R,6S)-2,6-dimethylpiperazine | HCID 6950261 | — |
| Reactant | HCID 86639070 | HCID 86639070 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67025565 | HCID 67025565 | — |
Reaction Steps
To a solution of 4-bromo-3-(thiomorpholinomethyl)benzaldehyde (0.73 g, 2.43 mmol) in dichloromethane (24.32 ml) was added (2R,6S)-2,6-dimethylpiperazine (0.416 g, 3.65 mmol). The mixture was allowed to stir at RT for 40 minutes before sodium triacetoxyborohydride (0.773 g, 3.65 mmol) was added. The reaction was stirred at RT for 2 hours. The mixture was diluted with dichloromethane and washed with saturated NaHCO3(aq), dried (MgSO4) and evaporated to give the sub-title compound as a pale yellow oil. Yield: 0.92 g
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08273774B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-32cc32c2dbc44750a163f69c65be418e |
| Source note | uspto-grants-2012_09 |