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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1449243Generated: October 27, 2026

Methanol → 4-(3-Methoxyphenyl)-1-methyl-3-methylidenepiperidin-2-one

https://huagongshe.com/reaction/1449243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 4-(3-methoxyphenyl)-1-methylpiperidine-3-carboxylateHCID 12947549—
SolventWaterHCID 962—
Product4-(3-Methoxyphenyl)-1-methyl-3-methylidenepiperidin-2-oneHCID 1294755093.1%

Reaction Steps

The ester ethyl 4-(3'-methoxyphenyl)-1-methylpiperidine-3-carboxylate (23)(5.0 g, 17.5 mmol), NaOH (1.49 g, 35 mmol), CH3OH (50 mL), and H2O (25 mL) were refluxed for 5 h. After the thorough removal of solvents, the residue was mixed with acetic anhydride (50 mL) and refluxed for 1 h, then cooled and evaporated and the crude reaction product partitioned between CHCl3 (50 mL) and saturated NaHCO3 (50 mL, pH 8). The aqueous layer was extracted with CHCl3 (2×50 mL) and the combined organic phases dried and evaporated. Distillation gave 3.77 g (92%) of 4-(3'-methoxyphenyl)-1-methyl-3-methylene-2-piperidone (24). Recrystallization (CH3Cl2 /hexane) gave the analytical sample: mp 67°-70° C: NMR δ 7.29 (m, 1H), 6.82 (m, 3H), 6.40 (t,J=2 Hz, 1H), 5.07 (t,J=2 Hz, 1H), 3.75 (s, 3H), 3.34 (m, 2H), 3.04 (s, 3H), 2.17 (m, 2H); IR (KBr) 1645, 1600 cm-1 ; mass spectrum m/e (real intensity) 231 (100), 216 (13). Anal. Calcd for C14H17NO2 : C, 72.7; H, 7.4; N, 6.1. Found: C, 72.6; H, 7.3; N, 6.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04189583
Source datasetuspto-grants-1980_02
ORD IDord-c21a0d582b1c471b96fc36f93ffa28af
Source noteuspto-grants-1980_02