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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 45806Generated: October 26, 2026

Formaldehyde → 4-(4-Methyl-1-piperazinyl)phenol

https://huagongshe.com/reaction/45806

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
Reactantp-(1-Piperazinyl)phenolHCID 92467—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventAcetic acid tetrahydrofuranHCID 23444217—
Product4-(4-Methyl-1-piperazinyl)phenolHCID 11622486106.4%

Reaction Steps

4-(piperazin-1-yl)phenol 2 g (11.24 mmol) and formaldehyde 4.5 ml (37% in water, 56 mmol) were suspended in a mixture of THF/AcOH 5/1 and stirred at room temperature. After 30 minutes, sodium triacetoxyborohydride 4.7 g (22.5 mmol) was added portion-wise. The reaction was let stir a few hours and evaporated down. The crude was purified on silica gel with ethyl acetate/ethanol/NH3 7 N in methanol 8/2/0.2 to give 2.3 g of pink solid as a free base. LC/MS (254 nm) HPLC method 2 Rt 2.4 min. 1H NMR (401 MHz, DMSO-d6) δ 8.78 (s, 1H), 6.71-6.84 (m, 2H), 6.56-6.69 (m, 2H), 2.85-3.03 (m, 4H), 2.46 (br. s., 4H), 2.23 (s, 3H). HRMS (ESI) calcd for C11H16N2O [M+H]+ 193.1336 Found 193.1328.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541576B2
Source datasetuspto-grants-2013_09
ORD IDord-3c74e94587be49a0ab3879cf6aab2ca3
Source noteuspto-grants-2013_09