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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1842900Generated: October 31, 2026

Ammonium Chloride → 1-(4-Bromo-2-fluorophenyl)cyclopropan-1-ol

https://huagongshe.com/reaction/1842900

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant4-Bromo-2-fluoro-benzoic acid methyl esterHCID 11345311—
ReactantHCID 178461634HCID 178461634—
CatalystHCID 178460666HCID 178460666—
SolventDiethyl EtherHCID 3283—
Product1-(4-Bromo-2-fluorophenyl)cyclopropan-1-olHCID 6266895728%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a stirred solution of Ti(OiPr)4 (44.68 mL, 141.63 mmol, 1 eq) in diethyl ether (250 mL) was added freshly prepared ethyl magnesium iodide (212.44 mL, 424.89 mmol, 3 eq) in diethyl ether (220 mL) at −78° C. for 45 min. The reaction mixture was stirred for 90 min at −78° C., then methyl 4-bromo-2-fluorobenzoate (33.0 g, 141.63 mmol, 1.0 eq) was added and the mixture allowed to stir at RT for 16 h. Saturated aqueous NH4Cl (30 mL) was added and the mixture passed through celite pad. The ether layer was separated, washed with 1 N HCl (250 mL), brine (500 mL), water (750 mL), dried over MgSO4 and the solvent evaporated. The resulting residue was purified by CC using PE/EtOAc (19:1) as eluent to get 1-(4-bromo-2-fluorophenyl)cyclopropanol (9.01 g, 28%; TLC system: PE/EtOAc (9:1), Rf: 0.3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946204B2
Source datasetuspto-grants-2015_02
ORD IDord-d3e02c0a2c4046c386ea68452455d3ad
Source noteuspto-grants-2015_02