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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26351Generated: October 26, 2026

Methanol → 1-Benzoyl-2-methyl-6-methoxypiperidine

https://huagongshe.com/reaction/26351

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantN-Benzoyl-2-methylpiperidineHCID 275047—
CatalystTetramethylammonium tetrafluoroborateHCID 12621—
Product1-Benzoyl-2-methyl-6-methoxypiperidineHCID 2132285477.6%

Reaction Steps

In the same manner as in Example 5, there are electrolyzed 43.8 g of 1-benzoyl-2-methylpiperidine and 60.2 g of methanol in the presence of 0.3 g of tetramethylammonium tetrafluoroborate as conducting salt. After throughput of 2.5 Faraday per mol of 1-benzoyl-2-methylpiperidine the current is switched off. After work-up of the electrolysis solution, 39.0 g of 1-benzoyl-2-methyl-6-methoxypiperidine (boiling point 78°-81° C./0.1 mm Hg; nD25 =1.5340) are obtained which corresponds to a product yield of 77.5% and a current efficiency of 62.0%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04149941
Source datasetuspto-grants-1979_04
ORD IDord-bfde8daec3d34f83be4c725b8a450688
Source noteuspto-grants-1979_04