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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2262490Generated: November 2, 2026

Formaldehyde → (4-Methylmorpholin-2-yl)methyl 4-phenylpiperazine-1-carboxylate

https://huagongshe.com/reaction/2262490

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantWaterHCID 962—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantMorpholin-2-ylmethyl 4-phenylpiperazine-1-carboxylate dihydrochloride saltHCID 66934509—
SolventMethanolHCID 887—
Product(4-Methylmorpholin-2-yl)methyl 4-phenylpiperazine-1-carboxylateHCID 4263400389%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851471B2
Source datasetuspto-grants-2010_12
ORD IDord-b74ea0d626d74368928de04ce63d3667
Source noteuspto-grants-2010_12