HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Bromotoluene → 3'-Methyl[1,1'-biphenyl]-3-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Bromotoluene | HCID 11560 | — |
| Reactant | 3-Bromobenzonitrile | HCID 23381 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3'-Methyl[1,1'-biphenyl]-3-carbonitrile | HCID 1393975 | 66.2% |
Reaction Conditions
| Temperature | 105 °C |
|---|
Reaction Steps
A mixture of 3-bromobenzonitrile (910 mg), Pd(Ph3P)4 (290 mg), (Me3Sn)2 (1.64 g) and dioxane (20 mL) was sealed under argon in a pressure tube. The tube was then heated at 100-110° C. for 3 hours with stirring and another 15 hours at 80° C. To the reaction mixture was added 1-bromo-3-methylbenzene (940 mg), Pd(PPh3)4 (290 mg) and dioxane (5 mL) under argon. The sealed tube was heated at 135-140° C. with stirring for two days. The catalyst was filtered off and the filtrate was poured into water and extracted with ethyl acetate (3×). The organic layer was washed with brine, dried over Mg2SO4, concentrated and purified on silica gel column (ethyl acetate/hexane, 1:3) to afford 0.64 g of 3-(3-cyanophenyl)-1-methylbenzene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06350761B1 |
| Source dataset | uspto-grants-2002_02 |
| ORD ID | ord-7e7471371ef84ed6b5916003de8fd24f |
| Source note | uspto-grants-2002_02 |