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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1893153Generated: November 1, 2026

Hydrochloric Acid → HCID 86659249, compound

https://huagongshe.com/reaction/1893153

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium ChlorideHCID 4873—
ReactantPotassium CarbonateHCID 11430—
Reactant3,3-Diethoxy-1-propeneHCID 62477—
ReactantHCID 44129579HCID 44129579—
CatalystTetrabutylammonium AcetateHCID 82707—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
ProductHCID 86659249HCID 8665924962.8%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of 1-bromo-4-(3-phenylpropyl)-benzene (684 mg, 2.48 mmol) in DMF (10 mL) were added acrolein diethyl acetal (1.7 mL, 11.1 mmol), tetrabutylammonium acetate (1.87 g, 6.2 mmol), potassium carbonate (514 mg, 3.72 mmol), potassium chloride (185 mg, 2.48 mmol), and palladium(II) acetate (50 mg, 0.22 mmol). After stirring at 90° C. for 4 h, the reaction mixture was cooled to RT and HCl (2M, 15 mL) was added. After stirring for 10 min at RT, the mixture was extracted with MTBE and washed with water and brine, dried over MgSO4 and concentrated under reduced pressure. Purification by MPLC (20% ethyl acetate in hexanes) gave 390 mg (2E)-3-[4-(3-phenylpropyl)phenyl]acrylaldehyde as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513220B2
Source datasetuspto-grants-2013_08
ORD IDord-b352cee2a5804257ba17f5c30b3f69e5
Source noteuspto-grants-2013_08