HuagongsheHuagongshe Chemistry Print Report · For research reference only
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
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-(2H-1,3-benzodioxol-5-yl)-5-methylimidazolidine-2,4-dione | HCID 2829817 | — |
| Reactant | 5-(4-Bromobutoxy)-4-propyl-1,1-bis(trifluoromethyl)-1,3-dihydroisobenzofuran | HCID 57900781 | — |
| Solvent | Water | HCID 962 | — |
| Product | 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 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07951822B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-ffd893985cdf44568a5b542a71223e0b |
| Source note | uspto-grants-2011_05 |