HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → HCID 54324094, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | (Methylsulfonyl)acetonitrile | HCID 75283 | — |
| Reactant | 4-Butoxybenzaldehyde | HCID 79813 | — |
| Catalyst | Piperidine | HCID 8082 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 54324094 | HCID 54324094 | 49% |
Reaction Steps
A mixture of 20.0 g (0.112 mol) of 4-butoxybenzaldehyde, 13.6 g (0.114 mol) of methylsulfonylacetonitrile, 8.9 g (0.11 mol) of pyridine, 4 drops of piperidine, and 100 mL of benzene were heated at reflux for 18 hr, with continuous azeotropic separation of the water evolved. Approximately half of the benzene was then distilled, and 50 mL of heptane was added. Upon cooling to room temperature, a white precipitate was formed, which was collected and recrystallized twice from toluene to afford 15.3 g (49%) of (5). A sample of (5) that was sublimed in vacuo melted at 96.5°-7° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05410630 |
| Source dataset | uspto-grants-1995_04 |
| ORD ID | ord-033b60020ff74f018c5586b12033b8c9 |
| Source note | uspto-grants-1995_04 |