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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552453Generated: October 30, 2026

Dimethylformamide → 5-(Benzo[d][1,3]dioxol-5-yl)-5-methyl-3-[4-[4-propyl-1,1-bis(trifluoromethyl)-1,3-dihydroisobenzofuran-5-yloxy]butyl]imidazolidine-2,4-dione

https://huagongshe.com/reaction/552453

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant5-(2H-1,3-benzodioxol-5-yl)-5-methylimidazolidine-2,4-dioneHCID 2829817—
Reactant5-(4-Bromobutoxy)-4-propyl-1,1-bis(trifluoromethyl)-1,3-dihydroisobenzofuranHCID 57900781—
SolventWaterHCID 962—
Product5-(Benzo[d][1,3]dioxol-5-yl)-5-methyl-3-[4-[4-propyl-1,1-bis(trifluoromethyl)-1,3-dihydroisobenzofuran-5-yloxy]butyl]imidazolidine-2,4-dioneHCID 44241289—

Reaction Steps

To a N,N-Dimethylformamide (2 mL) solution of 5-(4-bromobutoxy)-4-propyl-1,1-bis(trifluoromethyl)-1,3-dihydroisobenzofuran (25 mg, 0.0557 mmol), potassium carbonate mg, 0.111 mmol) and 5-(benzo[d][1,3]dioxol-5-yl)-5-methylimidazolidine-2,4-dione (CAS: 308122-40-9:DE335993) (19.6 mg, 0.0835 mmol) were added and the mixture was stirred overnight. The reaction solution was added with water and extracted with ethyl acetate. Subsequently, the organic layer was washed with saturated saline, dried using anhydrous sodium sulfate, and concentrated in vacuum. The residue was purified by thin-layer silica-gel column chromatography (hexane:ethyl acetate=2:1) and of the title compound (30.7 mg, 92%) was obtained as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07951822B2
Source datasetuspto-grants-2011_05
ORD IDord-ffd893985cdf44568a5b542a71223e0b
Source noteuspto-grants-2011_05