HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tosylacetonitrile → HCID 23047706, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tosylacetonitrile | HCID 79776 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | HCID 10753909 | HCID 10753909 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 23047706 | HCID 23047706 | — |
Reaction Steps
A mixture of 4.5 g (17.2 mmol) of 5-(4-chlorophenyl)pentyl bromide, 3.36 g (17.2 mmol) of (4-methylphenyl)sulfonylacetonitrile, 2.26 g (17.2 mmol) of 1,8-diazabicyclo(5,4,0)undec-7-ene and 30 ml of benzene is stirred at room temperature for 6 hours. Then the reaction mixture is washed with water; the organic phase is dried, and concentrated. The concentrate is chromatographed with a mixture of toluene and dioxane (10:1) on silica gel. Yield: 4.2 g (65% of theory) of the title compound, a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04933367 |
| Source dataset | uspto-grants-1990_06 |
| ORD ID | ord-9074b1b64ab44c1fabdba6ccab24ca47 |
| Source note | uspto-grants-1990_06 |