Back
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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-4-fluorobenzeneHCID 9993—
ReactantAmmonium ChlorideHCID 25517—
ReactantEthyl 5-bromovalerateHCID 84580—
ReactantMagnesiumHCID 5462224—
SolventDiethyl EtherHCID 3283—
Productalpha-(4-Bromobutyl)-4-fluoro-alpha-(4-fluorophenyl)benzenemethanolHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04968684
Source datasetuspto-grants-1990_11
ORD IDord-c9fc5c6731a5448d9140a3cf604f3e37
Source noteuspto-grants-1990_11