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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530623Generated: October 30, 2026

Formaldehyde → 4-Boc-1-methyl-2-phenylpiperazine

https://huagongshe.com/reaction/530623

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantTert-butyl 3-phenylpiperazine-1-carboxylateHCID 2735358—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
SolventSodium BicarbonateHCID 516892—
Product4-Boc-1-methyl-2-phenylpiperazineHCID 77180039101%

Reaction Steps

To a mixture of tert-butyl 3-phenylpiperazine-1-carboxylate (288 mg, 1.1 mmol), and formaldehyde (185 mg, 6.16 mmol) in methanol (7 mL) was added sodium triacetoxyborohydride (949 mg, 4.48 mmol) at 0° C. After stirring for 3 h at room temperature, the reaction mixture was diluted with 10% sodium bicarbonate solution and ethyl acetate. The aqueous part was extracted with ethyl acetate and the combined organic part was dried over sodium sulfate, filtered, concentrated in vacuo. The residue was purified by flash chromatography (20/1 dichloromethane/methanol) to provide 4-methyl-3-phenyl-piperazine-1-carboxylic acid tert-butyl ester (307 mg, 101%). (M+H)+=277 m/e. To a solution of 4-methyl-3-phenyl-piperazine-1-carboxylic acid tert-butyl ester (307 mg, 1.11 mmol) in THF (3 mL) at 0° C. was added 4M HCl in dioxane (0.9 mL). The reaction mixture was stirred overnight and concentrated in vacuo. The residue was triturated with dichloromethane and filtered to provide 1-methyl-2-phenyl-piperazine dihydrochloride (290 mg), which was used as is for the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09353096B2
Source datasetuspto-grants-2016_05
ORD IDord-83653501d9f14647b6cac6428c8e8740
Source noteuspto-grants-2016_05