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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 846748Generated: October 30, 2026

Benzene → HCID 15096756, compound

https://huagongshe.com/reaction/846748

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantDimethyl SulfateHCID 6497—
ReactantSodium HydroxideHCID 14798—
Reactant1-Benzyl-4,4-dimethoxypiperidin-3-olHCID 3019274—
CatalystBenzyl triethylammonium chlorideHCID 66133—
SolventWaterHCID 962—
ProductHCID 15096756HCID 15096756—

Reaction Steps

To a stirred mixture of 85 parts of 4,4-dimethoxy-1-(phenylmethyl)-3-piperidinol and 480 parts of sodium hydroxide solution 60% were added 288 parts of benzene and 0.5 parts of N,N,N-triethylbenzenemethanaminium chloride. Then there were added dropwise 49.2 parts of dimethyl sulfate at a temperature below 30° C. After stirring overnight at room temperature, there was added another portion of 13.3 parts of dimethyl sulfate and stirring was continued for 4 hours at room temperature. The reaction mixture was cooled, 640 parts of water were added and the layers were separated. The aqueous phase was extracted with benzene. The formed suspension was filtered and the filter-cake was set aside. The combined organic phases were washed with water, dried, filtered and evaporated. The oily residue was distilled (bp. 138° C. at 1 mm. pressure). The distillate was converted into the ethanedioate salt in 2-propanol. The salt was filtered off and crystallized from ethanol, yielding 34.9 parts of 3,4,4-trimethoxy-1-(phenylmethyl)piperidine ethanediote; mp. 180.6° C. (intermediate 58).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05137896
Source datasetuspto-grants-1992_08
ORD IDord-3155f9dbae8b4fef96f4d469ed217061
Source noteuspto-grants-1992_08