HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,4'-Difluorobenzophenone → HCID 21705161, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,4'-Difluorobenzophenone | HCID 67651 | — |
| Reactant | HCID 178418676 | HCID 178418676 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | HCID 21705161 | HCID 21705161 | — |
Reaction Steps
p-Fluorophenylmagnesium bromide (124 mL, 0.12 mol) was added dropwise to a stirring solution of 2,4′-difluorobenzophenone (24.5 g, 0.11 mol) in t-butylmethyl ether (100 mL) at rt. After the addition was complete the reaction was heated at reflux for 3 h. The solution was then cooled to rt and was poured in to ice cold 1.0 M HCl (aq) (100 mL). The organics were extracted with EtOAc (3×70 mL) and dried (Na2SO4). Concentration under reduced pressure gave the desired product bis(4-fluorophenyl)-2-fluorophenylmethanol as a pale yellow oil which was used in the next reaction without any further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06288122B1 |
| Source dataset | uspto-grants-2001_09 |
| ORD ID | ord-d115099f9d0349fe922b8ac45d5a3ab1 |
| Source note | uspto-grants-2001_09 |