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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2265157Generated: October 31, 2026

Benzyl Bromide → HCID 86614355, compound

https://huagongshe.com/reaction/2265157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 86071099HCID 86071099—
SolventDimethylformamideHCID 6228—
ProductHCID 86614355HCID 86614355—

Reaction Conditions

Temperature70 °C

Reaction Steps

540 mg of potassium carbonate and 0.25 mL of benzyl bromide were added to N,N-dimethylformamide (7 mL) solution of 453 mg of methyl (3RS,4SR)-4-o-tolyl-piperidine-3-carboxylate obtained in Production Example 31, and stirred at 70° C. for 1.5 hours. Then, this was restored to room temperature, aqueous saturated sodium hydrogencarbonate solution was added thereto and extracted with ether. The ether layer was washed with saturated saline water, and dried with anhydrous sodium sulfate, and the solvent was evaporated off under reduced pressure. The residue was separated and purified through silica gel column chroamtography (hexane/ethyl acetate=9/1) to obtain 463 mg of methyl (3RS,4SR)-1-benzyl-4-o-tolyl-piperidine-3-carboxylate. The compound was processed in the same manner as in Production Example 33-1 to obtain 360 mg of the entitled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855294B2
Source datasetuspto-grants-2010_12
ORD IDord-50fb1f0765114e7ca6d5615c1a90e67b
Source noteuspto-grants-2010_12