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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1851180Generated: November 1, 2026

Phenylacetaldehyde → HCID 67027749, compound

https://huagongshe.com/reaction/1851180

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetaldehydeHCID 998—
ReactantEthyl AcetateHCID 8857—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-Bromo-4-(dimethoxymethyl)benzeneHCID 688342—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67027749HCID 67027749—

Reaction Steps

A mixture of Mg turnings 2.4 g (0.1 mol) and 2 mL 1-bromo-4-(dimethoxymethyl)benzene (0.012 mol) in THF (100 mL) was heated under nitrogen atmosphere until the reaction starts. Subsequently additional 1-bromo-4-(dimethoxymethyl)benzene 14.71 mL (0.088 mol) dissolved in 30 mL THF was added slowly and the reaction refluxed for 1 h mixture to complete formation of the Gringnard reagent. A solution of 11.70 mL phenylacetaldehyde (0.1 mol) in 100 mL THF was added at to 0° C. and the reaction refluxed for 2 h upon completion of the addition. The mixture was worked up by pouring into saturated aqueous NH4Cl and extraction with ethyl acetate. The combined organic layers were washed with brine, dried over MgSO4 and the solvents were evaporated under reduced pressure. The brown-black oily product was used for the next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957064B2
Source datasetuspto-grants-2015_02
ORD IDord-eaae717bac734cc9b42a1ce7b7b3bb0e
Source noteuspto-grants-2015_02