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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243850Generated: October 30, 2026

1-Bromo-4-fluorobenzene → HCID 21929393, compound

https://huagongshe.com/reaction/1243850

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-4-fluorobenzeneHCID 9993—
ReactantAmmonium ChlorideHCID 25517—
ReactantMethyl methoxyacetateHCID 80507—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21929393HCID 21929393—

Reaction Conditions

Temperature60 °C

Reaction Steps

4.9 g of magnesium, 5 cm3 of 4-bromofluorobenzene and 25 cm3 of tetrahydrofuran are heated to a temperature in the region of 60° C. 17 cm3 of 4-bromofluorobenzene in solution in 25 cm3 of tetrahydrofuran are added and the mixture is heated at a temperature in the region of 60° C. for 2 hours. 5 cm3 of methyl methoxyacetate in solution in 25 cm3 of tetrahydrofuran are added to the solution prepared above, cooled to a temperature in the region of 0° C. After stirring for 24 hours at a temperature in the region of 20° C., the reaction mixture is poured into 200 cm3 of saturated aqueous ammonium chloride solution and extracted with three times 75 cm3 of ethyl acetate, and the organic phases are washed with twice 100 cm3 of distilled water, dried over magnesium sulphate and concentrated to dryness under reduced pressure. The residue obtained is purified by flash chromatography on silica gel (35–70 μm), eluting with pure dichloromethane; 9.8 g of 1,1-bis(4-fluorophenyl)-2-methoxyethanol are thus obtained in the form of a yellow oil, the characteristics of which are as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07119115B2
Source datasetuspto-grants-2006_10
ORD IDord-3c9ee98719d44da2a5e2ad737730080f
Source noteuspto-grants-2006_10