Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1094956Generated: November 2, 2026

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

https://huagongshe.com/reaction/1094956

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 numberUS08134006B2
Source datasetuspto-grants-2012_03
ORD IDord-899d9a055f15493999f43d6781808292
Source noteuspto-grants-2012_03