HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → Biphenyl-3-yl-dimethylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | N,N-Dimethyl-3-chloroaniline | HCID 23285 | — |
| Reactant | HCID 178418255 | HCID 178418255 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Biphenyl-3-yl-dimethylamine | HCID 12887384 | 94% |
Reaction Steps
Using a THF solution of phenylmagnesium bromide (1.19 mL, 1.01 M, 1.2 mmol) and 3-chloro-N,N-dimethylaniline (155.6 mg, 1.0 mmol) as starting materials, the reaction was performed at a scale of 1.0 mmol at 60° C. for 24 hours in the same manner as in Example 2. After performing silica gel column chromatography (toluene=50 and 100% in hexane), the above compound was obtained as a colorless liquid (0.185 g, yield=94%, purity=>98% (GC analysis)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08211820B2 |
| Source dataset | uspto-grants-2012_07 |
| ORD ID | ord-d32c24b7dbb440ab92469b3eaf049135 |
| Source note | uspto-grants-2012_07 |