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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 896253Generated: October 30, 2026

Acetic Acid → 5-Methoxy-4-[(1-methylpiperidin-4-yl)methoxy]-2-nitrobenzonitrile

https://huagongshe.com/reaction/896253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantFormaldehydeHCID 712—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant2-Nitro-4-(1-piperidin-4-ylmethoxy)5-methoxybenzonitrileHCID 22349625—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product5-Methoxy-4-[(1-methylpiperidin-4-yl)methoxy]-2-nitrobenzonitrileHCID 2234962086.3%

Reaction Steps

2-nitro-4-(1-piperidin-4-ylmethoxy)5-methoxybenzonitrile (771 mg, 2.65 mmol) in CH2Cl2 (8 ml) and MeOH (4 ml) was reacted for 0.5 hour with formaldehyde (13.3 M, 300 μl, 4 mmol), acetic acid (191 mg, 3.18 mmol) and NaBH(OAc)3 (674 mg, 3.18 mmol) slowly added over 15 minutes. The solution was evaporated, the oily residue was taken up in a mixture of Na2CO3 and ethylacetate, extracted with ethylacetate. The organic phase was dried over MgSO4, evaporated to give title compound as a yellow solid (698 mg, 86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06919338B2
Source datasetuspto-grants-2005_07
ORD IDord-1823650ebc5347afa4eeed4ebba104ff
Source noteuspto-grants-2005_07