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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198720Generated: October 26, 2026

Dimethylformamide → 2-(1-Methylbutyloxy)-3-dimethylaminoacrolein

https://huagongshe.com/reaction/1198720

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(4-Methylbutyloxy)acetaldehyde diethylacetalHCID 19930625—
Solvent1,1-DichloroethaneHCID 6365—
Product2-(1-Methylbutyloxy)-3-dimethylaminoacroleinHCID 53907798—

Reaction Conditions

Temperature5 °C

Reaction Steps

A solution prepared by adding 30 g of dried N,N-dimethylformamide to dried dichloroethane was cooled to 5° C. or lower. After a solution containing 63 g of phosphorus oxychlorate dissolved in dichloroethane was added to the cooled solution dropwise, the mixture was stirred for 30 minutes at 5° C. or lower. Subsequently, to the reaction solution was added a dichloroethane solution of the compound (54), and the resulting mixture was stirred for 30 minutes at room temperature and then for one hour at 70° C. After the reaction solution was cooled to room temperature, the reaction solution was poured into ice water and was then made basic by addition of potassium carbonate. The reaction solution was then concentrated under reduced pressure. The concentrate was warmed and stirred, and was then extracted with ethyl acetate. After the extract was dried over magnesium sulfate, the solvent used was distilled out. The residue was distilled under reduced pressure to obtain 2-(1-methylbutyloxy)-3-dimethylaminoacrolein (55) (boiling point: 150° to 155° C./5 mmHg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05281685
Source datasetuspto-grants-1994_01
ORD IDord-bfdf6a97dcdc45ae86e3840c048a7cfe
Source noteuspto-grants-1994_01