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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743203Generated: November 3, 2026

Water → HCID 22238270, compound

https://huagongshe.com/reaction/1743203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-Benzylpiperidine-4-carbaldehydeHCID 89584—
Reactant1-Bromo-2,5-dimethoxy-3,4,6-trimethylbenzeneHCID 297365—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22238270HCID 2223827052.5%

Reaction Steps

n-Butyllithium (1.6 M, 19.5 mL, 31.2 mmol) was added to a solution of 1-bromo-2,5-dimethoxy-3,4,6-trimethylbenzene (8.00 g, 30.87 mmol) in tetrahydrofuran (80 mL) at −78° C., and the mixture was stirred for 30 minutes at the same temperature. To the reaction mixture was added 1-benzyl-4-formylpiperidine (6.23 g, 30.65 mmol). The mixture was stirred for 30 minutes at room temperature, then poured into water, and extracted twice with ethyl acetate. The organic layers were combined, washed with an aqueous saturated sodium hydrogencarbonate, dried over magnesium sulfate, filtered, and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography (ethyl acetate) to obtain the title compound (6.17 g, yield 52%). This was oily.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07008950B1
Source datasetuspto-grants-2006_03
ORD IDord-f015fa04af5e44eaa8baffc458286c18
Source noteuspto-grants-2006_03