HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → (E)-3-(3-t-Butyl-4-hydroxyphenyl)-2-(4-fluorophenylsulfonyl)acrylonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2-(4-Fluorobenzenesulfonyl)acetonitrile | HCID 565732 | — |
| Reactant | 3-(tert-Butyl)-4-hydroxybenzaldehyde | HCID 3017618 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (E)-3-(3-t-Butyl-4-hydroxyphenyl)-2-(4-fluorophenylsulfonyl)acrylonitrile | HCID 22000567 | 82.2% |
Reaction Steps
The reaction mixture of 178.0 mg of 3-t-butyl-4-hydroxybenzaldehyde and 219.0 mg of (4-fluorobenzenesulphonyl)acetonitrile in 2.0 mL of ethanol containing 0.01 mL piperidine was refluxed for 4 h and cooled down. To the above reaction mixture was added water and then the aqueous layer was extracted with ethyl acetate. The organic layer was washed with brine, dried over magnesium sulfate and concentrated. The resulting residue was purified on silica gel column eluting with ethyl acetate-hexane (1:6) to give 295.0 mg of the titled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06225346B1 |
| Source dataset | uspto-grants-2001_05 |
| ORD ID | ord-0ff9b479bb8a45d2b56a8c064abba708 |
| Source note | uspto-grants-2001_05 |