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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 981313Generated: October 29, 2026

Methyl Isobutyl Ketone → trans-3-methoxy-N,N,gamma-trimethyl-alpha,alpha-diphenyl-4-[[3-(trifluoromethyl)benzoyl]amino]-1-piperidinebutanamide

https://huagongshe.com/reaction/981313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl Isobutyl KetoneHCID 7909—
ReactantSodium CarbonateHCID 10340—
ReactantN-(dihydro-5-methyl-3,3-diphenyl-2(3H)-furanylidene)-N-methylmethanaminium bromideHCID 20071674—
Reactanttrans-N-(3-methoxy-4-piperidinyl)-3-(trifluoromethyl)benzamideHCID 67928786—
SolventWaterHCID 962—
Producttrans-3-methoxy-N,N,gamma-trimethyl-alpha,alpha-diphenyl-4-[[3-(trifluoromethyl)benzoyl]amino]-1-piperidinebutanamideHCID 13171677922.5%

Reaction Steps

A mixture of 3.0 parts of trans-N-(3-methoxy-4-piperidinyl)-3-(trifluoromethyl)benzamide, 2.65 parts of sodium carbonate and 80 parts of 4-methyl-2-pentanone was stirred for 30 minutes at reflux temperature, using a water separator. After cooling 3.96 parts of N-(dihydro-5-methyl-3,3-diphenyl-2(3H)-furanylidene)-N-methylmethanaminium bromide were added and stirring was continued for 5 hours at reflux. After cooling overnight at room temperature, the reaction mixture was washed twice with 50 parts of water, dried, filtered and evaporated in vacuo. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from 8 parts of acetonitrile. The product was filtered off and dried, yielding 1.3 parts (22.5%) of trans-3-methoxy-N,N,γ-trimethyl-α,α-diphenyl-4-[[3-(trifluoromethyl)benzoyl]amino]-1-piperidinebutanamide; mp. 197.8° C. (compound 52).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04990521
Source datasetuspto-grants-1991_02
ORD IDord-e28060d469d34850b2d695b0b684ef29
Source noteuspto-grants-1991_02