HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → Butyrophenone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 3-Tolunitrile | HCID 12104 | — |
| Reactant | HCID 178461630 | HCID 178461630 | — |
| Product | Butyrophenone | HCID 10315 | — |
Reaction Steps
To a 0° C. solution of EtMgBr in Et2O (3.0M, 570 mL, Aldrich) was slowly added m-tolunitrile (102 mL, Aldrich). After stirring at r.t. for 19 hr., benzene (300 mL) was added and the resulting mixture was cooled to 0° C. HCl (6N, 600 mL) was then slowly added. The organic phase was separated, washed with 5% NaHCO3 and brine, dried (MgSO4) and evaporated to afford the desired ketone as a yellow liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05424320 |
| Source dataset | uspto-grants-1995_06 |
| ORD ID | ord-a1fada7721ab431fa350d373a4b94879 |
| Source note | uspto-grants-1995_06 |