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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719113Generated: October 29, 2026

Thionyl bromide → 1-(Bromomethyl)-4-(2-chloroethoxy)benzene

https://huagongshe.com/reaction/719113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl bromideHCID 68176—
Reactant[4-(2-Chloroethoxy)phenyl]methanolHCID 21882321—
SolventDiethyl EtherHCID 3283—
Solvent1,4-DioxaneHCID 31275—
Product1-(Bromomethyl)-4-(2-chloroethoxy)benzeneHCID 2188225258%

Reaction Steps

To 4-(2-Chloroethoxy)benzylalcohol CAS No. [111728–87-1] (6.4 g, 34.31 mmol) in dioxane (100 mL) at 0° C. was added slowly thionylbromide (7.13 g, 34.31 mmol). The reaction was run at 0° C. after 5 min. The reaction mixture was diluted with ether (200 mL) and washed with H2O (1×30 mL) then NaHCO3 (2×25 mL), and brine (30 mL). The organic extract was dried over MgSO4 and concentrated. The crude product was purified by silica gel chromatography (15% EtOAc/Hex) to yield 5.0 g (58%) of the desired product. Mp=64–66° C.; 1H NMR (DMSO) 7.37 (d, 2H, J=8.8 Hz), 6.93 (d, 2H, J=8.8 Hz), 4.68 (s, 2H), 4.24 (t, 2H, J=5.05 Hz), 3.93 (t, 2H, J=5.27 Hz); MS eI m/z 248 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07132417B2
Source datasetuspto-grants-2006_11
ORD IDord-ec6f81e5a777434484b1b9ed1793558d
Source noteuspto-grants-2006_11