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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 885854Generated: November 3, 2026

Formaldehyde → 1-[3-((3R,5S)-3,4,5-trimethyl-piperazin-1-yl)-phenyl]-ethanone

https://huagongshe.com/reaction/885854

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantAmmonium HydroxideHCID 14923—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactantcis-1-[3-(3,5-Dimethyl-piperazin-1-yl)-phenyl]-ethanoneHCID 67049822—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductAmmonium HydroxideHCID 149233%
Product1-[3-((3R,5S)-3,4,5-trimethyl-piperazin-1-yl)-phenyl]-ethanoneHCID 58208360156.7%

Reaction Steps

A mixture of 1-[3-((3R,5S)-3,5-dimethyl-piperazin-1-yl)-phenyl]-ethanone (226 mg, 0.974 mmol), NaBH(OAc)3 (309 mg, 1.46 mmol) and CH2O (37% water solution, 0.087 ml, 1.17 mmol) in DCM (10 ml) was stirred at room temperature overnight. The resulting solution was diluted with water, brought to basic conditions with NH4OH and extracted with DCM. The organic phase was dried over Na2SO4 and evaporated in vacuo. The crude reaction mixture was purified by SCX cartridge (eluent: MeOH and then 3% NH4OH in MeOH) to give 188 mg of 1-[3-((3R,5S)-3,4,5-trimethyl-piperazin-1-yl)-phenyl]-ethanone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08242175B2
Source datasetuspto-grants-2012_08
ORD IDord-c9557b043568477b80db5b3e20f9eded
Source noteuspto-grants-2012_08