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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1092060Generated: October 27, 2026

Acetic Acid → Methyl 4-(1-methylpiperidin-4-YL)benzoate

https://huagongshe.com/reaction/1092060

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantFormaldehydeHCID 712—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantMethyl 4-piperidin-4-ylbenzoate hydrochlorideHCID 57440410—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 4-(1-methylpiperidin-4-YL)benzoateHCID 4976014450.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

Water (0.2 mL), paraformaldehyde (0.470 g, 15.64 mmol) and acetic acid (0.895 mL, 15.64 mmol) were added to a stirred suspension of 4-(4-(methoxycarbonyl)phenyl)piperidinium chloride (1 g, 3.91 mmol) in THF (20 mL) under nitrogen. Sodium cyanoborohydride (0.369 g, 5.87 mmol) was added portionwise over a period of 10 mins. The resulting mixture was stirred at 60° C. for 19 h. The reaction mixture was evaporated to dryness and mixed with water (20 mL) and 1M HCl (5 mL). The solution was washed with EtOAc (2×15 mL), basified with K2CO3 and extracted with EtOAc (2×15 mL). The organic layer was washed with saturated brine and dried over MgSO4, filtered and evaporated to afford pure methyl 4-(1-methylpiperidin-4-yl)benzoate (0.459 g, 50.4%) as a colourless oil which crystallised on standing.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129391B2
Source datasetuspto-grants-2012_03
ORD IDord-55c72fd926f24e59a2496371ab83f75d
Source noteuspto-grants-2012_03