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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1954882Generated: November 1, 2026

Hydrogen Bromide → 2-Fluorophenethyl bromide

https://huagongshe.com/reaction/1954882

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantSulfuric AcidHCID 1118—
Reactant2-(2-Fluorophenyl)ethan-1-olHCID 2733296—
Product2-Fluorophenethyl bromideHCID 2756964—

Reaction Steps

To a mixture of aqueous hydrobromic acid (48%, 360 mL) and concentrated sulfuric acid (103.6 mL) at room temperature was added dropwise 2-(2-fluorophenyl)ethanol (250 g, 1.78 mol, Aldrich). The reaction mixture was refluxed for 7 h, poured onto 600 ml of ice and the mixture was extracted with diethyl ether. The diethyl ether extracts were washed successively with saturated sodium carbonate and brine. The organic phase was dried (MgSO4) and concentrated in vacuo to give 359.9 g (99%) of 2-(2-fluorophenyl-ethylbromide as a brown oil. This product was used without further purification. NMR (CDCl3 : d 7.6-6.9 (m, 4H, ArH), 3.6 (t, 2H, CH2), 3.2 (t, 2H, CH2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06124284
Source datasetuspto-grants-2000_09
ORD IDord-ac5ddeabd91243d4b6f5792cb65feea7
Source noteuspto-grants-2000_09