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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2208673Generated: October 30, 2026

Acetaldehyde → Methyl 3-{[(2R*,6S*)-1-benzyl-2,6-dimethylpiperidin-4-yl](ethyl)amino}-2-methyl-5-(trifluoromethyl)benzoate

https://huagongshe.com/reaction/2208673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantMethyl 3-{[(2R*,6S*)-1-benzyl-2,6-dimethylpiperidin-4-yl]amino}-2-methyl-5-(trifluoromethyl)benzoateHCID 70874011—
SolventAcetic AcidHCID 176—
SolventChloroformHCID 6212—
ProductMethyl 3-{[(2R*,6S*)-1-benzyl-2,6-dimethylpiperidin-4-yl](ethyl)amino}-2-methyl-5-(trifluoromethyl)benzoateHCID 8671953344%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of methyl 3-{[(2R,6S)-1-benzyl-2,6-dimethylpiperidin-4-yl]amino}-2-methyl-5-(trifluoromethyl)benzoate (223 mg, 0.513 mmol) in chloroform (4 mL) and acetic acid (500 uL) was added acetaldehyde (1.0 ml) and stirred for 30 min at 0° C. Then sodium triacetoxyborohydride (343 mg, 1.54 mmol) was added to the reaction mixture at 0° C. The reaction mixture was stirred at 23° C. for 4 hours. Then the reaction mixture was quenched with aq. NaHCO3 until pH8-9. The content was extracted with ethylacetate. The organic layer was washed with brine. The organic layer was dried over MgSO4 and filtered. The filtrate was concentrated in vacuo. The residue was purified by silica gel column chromatography (heptane/ethylacetate=4/1 to 1/2) to give the titled compound as a colorless oil. (105.5 mg, 44% yield). MS (ES) [M+H] 463.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376422B2
Source datasetuspto-grants-2016_06
ORD IDord-922218ab936f46a9bcd54ebedef3be6c
Source noteuspto-grants-2016_06