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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1070718Generated: November 2, 2026

Hydrochloric Acid → HCID 12988961, compound

https://huagongshe.com/reaction/1070718

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantButyl vinyl etherHCID 8108—
Reactant1,3-Bis(diphenylphosphino)propaneHCID 81219—
ReactantHCID 12988960HCID 12988960—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductHCID 12988961HCID 12988961—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirred solution of trifluoro-methanesulfonic acid 3-(1-propyl-piperidin-4-yl)-phenyl ester (300 mg) in DMF (4 ml) under argon atm at r.t. was subsequently added NEt3 (356 μL), butyl vinyl ether (823 μL), 1,3-bis(diphenylphosphino)propane (50 mg), and Pd(OAc)2 (19 mg). The reaction mixture was then heated to 80° C. and after 2 h the reaction was stopped. 5% Hydrochloric acid solution (6 ml) was added and the combined mixture stirred for 45 min. Then CH2Cl2 was added and the phases were separated. The aqueous layer was then extracted with CH2Cl2. The combined organic phases were dried (MgSO4), filtered and evaporated to dryness. The crude product was purified by flash chromatography (MeOH:CH2Cl2 (1:9 (v/v)). Collection of the fractions containing pure product and evaporation of the solvent afforded pure 1-[3-(1-Propyl-piperidin-4-yl)-phenyl]-ethanone (35 mg). MS m/z (rel. intensity, 70 eV) 245 (M+, 4), 216 (bp), 100 (19), 70 (36), 57 (13).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06903120B2
Source datasetuspto-grants-2005_06
ORD IDord-387439f4bee64df1966f38a110528ef3
Source noteuspto-grants-2005_06