HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4-Formyl-3-[(1-methylethyl)sulfonyl]benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) | HCID 466102 | — |
| Reactant | 4-(1,3-Dioxan-2-yl)-3-(propan-2-ylsulfonyl)benzonitrile | HCID 58133807 | — |
| Solvent | Propan-2-one--water (1/1) | HCID 18366337 | — |
| Product | 4-Formyl-3-[(1-methylethyl)sulfonyl]benzonitrile | HCID 58133848 | — |
Reaction Conditions
| Temperature | 165 °C |
|---|
Reaction Steps
In an Emrys microwave, 4-(1,3-dioxan-2-yl)-3-(propan-2-ylsulfonyl)benzonitrile (1090 mg, 3.7 mmol) and pyridinium 4-toluenesulfonate (696 mg, 2.8 mmol; 0.75 eq.) in acetone/water (1:1, 15 ml) were heated with stirring at 165° C. for 7 min. The reaction mixture was then added to water (150 ml) and extracted with dichloromethane (9×30 ml). The combined organic phases were subsequently washed with saturated sodium chloride solution (30 ml), dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude product was subjected to flash chromatography on silica gel (mobile phase: cyclohexane→cyclohexane/ethyl acetate 3:2). The title compound was isolated as a solid (0.764 g, 87% of theory).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08288402B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-09d4b09181a44fc6913e67e9aab5fb99 |
| Source note | uspto-grants-2012_10 |