HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Cyanide → HCID 54307398, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 4-Fluorobenzaldehyde | HCID 68023 | — |
| Reactant | HCID 54071145 | HCID 54071145 | — |
| Reactant | HCID 54283396 | HCID 54283396 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 54307398 | HCID 54307398 | — |
Reaction Steps
To 3-bromomethyl-4-(4-(methylthio)phenyl)-5-phenyl-thiopene-2-carboxylic acid methyl ester (1 g, prepared by using the same procedure described for 3-bromomethyl-5-(fluorophenyl)-4-(4-(methylthio)phenyl)thiophene-2-carboxylic acid methyl ester of Example 8, Step 2 but substituting benzaldehyde for 4-fluorobenz-aldehyde) in DMSO (25 mL) in an ice bath was added powdered KCN. The mixture was stirred for 15 minutes at R.T., then H2O was added and the mixture was extracted with Et2O (2×), the organic layers were combined, washed with brine, dried over MgSO4, filtered and the solvent was evaporated under vacuum. Purification by silica gel chromatography afforded the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05521213 |
| Source dataset | uspto-grants-1996_05 |
| ORD ID | ord-626300a690bb480d988f49f837db5bb8 |
| Source note | uspto-grants-1996_05 |