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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473365Generated: October 30, 2026

Acetaldehyde → HCID 57515866, compound

https://huagongshe.com/reaction/473365

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
ReactantPiperidineHCID 8082—
ReactantHCID 57515867HCID 57515867—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57515866HCID 57515866—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a stirred solution of piperidine, 2,2,6,6-tetramethyl-(9.2 ml, 54 mmol) in THF (400 ml) at −78° C. was added butyllithium (˜2.5 m in toluene; 18 ml, 45 mmol) dropwise. The reaction was then stirred at 0° C. for 5 min at −78° C., and a solution of 5-(methoxymethoxy)-2-(trifluoromethyl)pyridine (7.5 g, 36 mmol) in THF (100 ml) was added dropwise. The mixture was stirred for an additional 10 min, then acetaldehyde (20 ml, 362 mmol) was added and stirring continued for 15 min. the reaction was slowly quenched with H2O, warmed to RT, extracted with EtOAc (3×), combine organic layers were dried over MgSO4, filtered, concentrated and the crude product was purified by ISCO (20% EtOAc/Hexanes) to give the title compound as a light yellow solid. MS (m+1): 252.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633315B2
Source datasetuspto-grants-2014_01
ORD IDord-2d4076b394ea4b96be3b00c2d951bc64
Source noteuspto-grants-2014_01