HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073167Generated: October 30, 2026
1-Bromo-4-fluorobenzene → alpha-(4-Bromobutyl)-4-fluoro-alpha-(4-fluorophenyl)benzenemethanol
https://huagongshe.com/reaction/1073167
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromo-4-fluorobenzene | HCID 9993 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Ethyl 5-bromovalerate | HCID 84580 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | alpha-(4-Bromobutyl)-4-fluoro-alpha-(4-fluorophenyl)benzenemethanol | HCID 14722555 | — |
Reaction Steps
To a stirred and refluxing Grignard complex previously prepared starting from 280 parts of 1-bromo-4-fluorobenzene, 34.6 parts of magnesium and 392 parts of 1,1'-oxybisethane, was added dropwise a solution of 116 parts of ethyl 5-bromopentanoate in 392 parts of 1,1'-oxybisethane. Upon complete addition, stirring was continued for 4 hours at reflux temperature. The reaction mixture was decomposed with a saturated ammonium chloride solution and the product was extracted with 1,1'-oxybisethane. The extract was dried, filtered and evaporated. The residue was triturated in hexane. The latter was decanted and the residue was crystallized from hexane. The product was filtered off and dried at room temperature, yielding 100 parts of α-(4-bromobutyl)-4-fluoro-α-(4-fluorophenyl)benzenemethanol; mp. 55° C. (int. 49).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04968684 |
|---|
| Source dataset | uspto-grants-1990_11 |
|---|
| ORD ID | ord-c9fc5c6731a5448d9140a3cf604f3e37 |
|---|
| Source note | uspto-grants-1990_11 |
|---|