HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Bis(4-fluorophenyl)(phenyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4,4'-Difluorobenzophenone | HCID 9582 | — |
| Reactant | HCID 178418255 | HCID 178418255 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | Bis(4-fluorophenyl)(phenyl)methanol | HCID 12580270 | — |
Reaction Steps
Phenylmagnesium bromide (100 mL, 0.1 mol) was added dropwise to a stirring solution of 4,4′-difluorobenzophenone (20 g, 0.092 mol) in t-butylmethyl ether (150 mL) at rt. After the addition was complete the reaction was heated at reflux for 3 h. The solution was cooled to rt and was poured in to ice cold aqueous 1.0 M HCl (100 mL). The organics were extracted with EtOAc (2×50 mL) and dried (Na2SO4). Concentration under reduced pressure gave bis(4-fluorophenyl)phenylmethanol as a pale brown oil. After drying in vacuo for 2 h the crude material 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-ea4298662896447ab9e93d2f7401f237 |
| Source note | uspto-grants-2001_09 |