HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → (4-Methylmorpholin-2-yl)methyl 4-phenylpiperazine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | Morpholin-2-ylmethyl 4-phenylpiperazine-1-carboxylate dihydrochloride salt | HCID 66934509 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (4-Methylmorpholin-2-yl)methyl 4-phenylpiperazine-1-carboxylate | HCID 42634003 | 89% |
Reaction Steps
Morpholin-2-ylmethyl 4-phenylpiperazine-1-carboxylate (non-HCl salt of Example 10; 1.00 g, 3.27 mmol) and 37% formaldehyde in water (1.97 g, 1.82 mL, 65.5 mmol) were dissolved in MeOH (20 mL) at room temperature followed by addition of sodium triacetoxyborohydride (2.78 g, 13.1 mmol) portionwise over 5 minutes. The reaction mixture was stirred for 2 h. The reaction mixture was quenched by the addition of saturated aq Na2CO3 solution. The solvents were removed in vacuo and the residual aqueous phase was loaded onto an Isolute HM-N 20 mL cartridge. The desired product was eluted with DCM (200 mL) and the solvent removed in vacuo to give (4-methylmorpholin-2-yl)methyl 4-phenylpiperazine-1-carboxylate (0.93 g, 88.9%) as a colourless gum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07851471B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-b74ea0d626d74368928de04ce63d3667 |
| Source note | uspto-grants-2010_12 |