Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361726Generated: October 30, 2026

Dichloromethane → N-(4-[1,3]dioxolan-2-yl-2,5-dimethylphenyl)acrylamide

https://huagongshe.com/reaction/1361726

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantAcryloyl chlorideHCID 13140—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 57461076HCID 57461076—
SolventWaterHCID 962—
ProductN-(4-[1,3]dioxolan-2-yl-2,5-dimethylphenyl)acrylamideHCID 5746107797%

Reaction Steps

To a 500 mL round-bottom flask was added crude 4-[1,3]dioxolan-2-yl-2,5-dimethylphenylamine (5.6 g, 29 mmol), dichloromethane (100 mL) and diisopropylethylamine (7.6 mL, 43.5 mmol). The resulting mixture was stirred at room temperature until the ingredients dissolved and then the mixture was cooled to 0° C. Acryloyl chloride (2.35 mL, 29 mmol) was then added dropwise over a 5 minute period. The reaction mixture was stirred at 0° C. to 5° C. for 1 hour and then water (50 mL) was added and stirring was continued for about 30 minutes at which time fine solids had formed. The mixture was filtered to collect the solids. The layers of the filtrate were then separated and the organic layer was concentrated under reduced pressure to dryness. Dichloromethane (50 mL) was added to the residue and this mixture was stirred until a free-flowing slurry developed. The slurry was filtered (using the same funnel used to collect the fine solids above) and the filter cake was washed with dichloromethane (10 mL) and dried to provide N-(4-[1,3]dioxolan-2-yl-2,5-dimethylphenyl)acrylamide (3.1 g, 97% purity) as a white to off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07880010B2
Source datasetuspto-grants-2011_02
ORD IDord-3974d741ae1943d4a86d158ac485bbf0
Source noteuspto-grants-2011_02