Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1415827Generated: October 25, 2026

1,2-Dibromoethane → 3-(3,4-Dimethylbenzoyl)-2-methylpropionaldehyde ethylene acetal

https://huagongshe.com/reaction/1415827

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DibromoethaneHCID 7839—
ReactantAmmonium ChlorideHCID 25517—
ReactantMagnesiumHCID 5462224—
ReactantHCID 14383752HCID 14383752—
ReactantN-Methoxy-N,3,4-trimethylbenzamideHCID 14973055—
SolventTetrahydrofuranHCID 8028—
Product3-(3,4-Dimethylbenzoyl)-2-methylpropionaldehyde ethylene acetalHCID 2186283139%

Reaction Steps

0.29 ml (3.4 mmol) of 1,2-dibromoethane was added to a suspension of 1.66 g (68.1 mmol) of magnesium in 5 ml of anhydrous tetrahydrofuran under a stream of nitrogen. 9.96 g (51.1 mmol) of 3-bromo-2-methylpropionaldehyde ethylene acetal [prepared as described in step (i) above] were then added dropwise to the resulting mixture, whilst ice-cooling, after which the mixture was stirred for 1 hour. A solution of 6.58 g (34.1 mmol) of N-methoxy-N-methyl-3,4-dimethylbenzamide in 30 ml of tetrahydrofuran was then added dropwise to the mixture, and the resulting mixture was stirred, whilst ice-cooling for 1 hour. A saturated aqueous solution of ammonium chloride was then added to the mixture, and the resulting mixture was extracted twice with ethyl acetate. The organic extracts were combined and washed with a saturated aqueous solution of sodium chloride, after which they were dried over anhydrous magnesium sulfate and concentrated by evaporation under reduced pressure. The residue thus obtained was applied to a silica gel chromatography column and eluted with a 6:1 by volume mixture of hexane and ethyl acetate, to give 3.26 g (yield 39%) of the title compound as a colorless oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05908858
Source datasetuspto-grants-1999_06
ORD IDord-0f88ab90ee4946f490b129062cec3d03
Source noteuspto-grants-1999_06