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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2166619Generated: November 3, 2026

Acetone → 1-Benzyl-3-[2-benzyloxy-4-(1,1-dimethylheptyl)phenyl]-4-piperidone

https://huagongshe.com/reaction/2166619

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantSulfuric AcidHCID 1118—
ReactantAmmonium HydroxideHCID 14923—
Reactant1-Benzyl-3-[2-benzyloxy-4-(1,1-dimethylheptyl)phenyl]-4-piperidinolHCID 20499775—
Catalystchromium (VI) trioxideHCID 10219390—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product1-Benzyl-3-[2-benzyloxy-4-(1,1-dimethylheptyl)phenyl]-4-piperidoneHCID 20499783—

Reaction Conditions

Temperature18 °C

Reaction Steps

To a cooled solution of 24.8 g. (50 mmols.) of 1-benzyl-3-[2-benzyloxy-4-(1,1-dimethylheptyl)phenyl]-4-piperidinol, 100 ml. of acetone, 6.0 g. (60 mmols.) of chromium trioxide, 15 ml. of water and 20 ml. of acetic acid is added dropwise 20 ml. of concentrated sulfuric acid at such a rate as to maintain the temperature at 5° C. The reaction mixture is stirred 5 hours longer (t<18° C.) and then neutralized with concentrated ammonium hydroxide. The reaction mixture is extracted with 500 ml. of ether, the ether extract washed once with saturated sodium chloride, dried over magnesium sulfate and evaporated Purification is accomplished via rapid column chromatography on 100 g. of silica gel eluted with ether to yield the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04387229
Source datasetuspto-grants-1983_06
ORD IDord-e66addc1db514811bc4654553dc336d0
Source noteuspto-grants-1983_06