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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2196092Generated: November 1, 2026

Trimethyl orthoformate → 1-Acetyl-4,4-dimethoxy-piperidine

https://huagongshe.com/reaction/2196092

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl orthoformateHCID 9005—
ReactantN-Acetyl-4-piperidoneHCID 122563—
Catalystp-Toluenesulfonic acid monohydrateHCID 521998—
CatalystSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
Product1-Acetyl-4,4-dimethoxy-piperidineHCID 1265364689.2%

Reaction Steps

A solution of 1-acetyl-4-piperidone (17.0 g, 121 mmol), trimethyl orthoformate (26.4 mL, 241 mmol) and para-toluenesulfonic acid monohydrate (80 mg, 0.42 mmol) in dry methanol (34 mL) was refluxed for one hour. Then 1.0 M methanolic NaOMe (0.42 mL, 0.42 mmol) and excess of methanol and trimethyl orthoformate were removed by distillation (atmospheric pressure). Further distillation under reduced pressure afforded 1-acetyl-4,4-dimethoxy-piperidine (20.2 g, 89%) 1H NMR (DMSO) δ 3.45-3.32 (m, 4H), 3.10 (s, 6H), 1.99 (s, 3H), 1.72-1.62 (m, 2H), 1.61-1.52 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338431B2
Source datasetuspto-grants-2012_12
ORD IDord-4a56d7b9dea5446f82ab7ca68dcaa477
Source noteuspto-grants-2012_12