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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 583828Generated: October 26, 2026

Thionyl bromide → 4-(3-Chloropropoxy)-benzyl bromide

https://huagongshe.com/reaction/583828

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl bromideHCID 68176—
Reactant4-(3-Chloropropoxy)benzyl alcoholHCID 22897496—
SolventDiethyl EtherHCID 3283—
Solvent1,4-DioxaneHCID 31275—
Product4-(3-Chloropropoxy)-benzyl bromideHCID 21882276—

Reaction Steps

A solution consisting of 4-(3-chloropropoxy)-benzyl alcohol No. 162 (10.6 g, 52.8 mmol) in dioxane (0.125 l) was cooled to 0° C. and treated with a dropwise addition of thionyl bromide (12.0 g, 58.0 mmol). After 10 minutes the reaction was complete. The dioxane was diluted with ethyl ether and washed with water, brine, and then dried over MgSO4. The material was concentrated down to yield 15 g of an oil: 1H NMR (DMSO) 7.36 (d, 2 H, J=8.8 Hz), 6.92 (d, 2 H, J=8.6 Hz), 4.68 (s, 2 H), 4.08 (t, 2 H, J=5.9 Hz), 3.77 (t, 2 H, J=6.4 Hz); MS (FAB) 266 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06924281B2
Source datasetuspto-grants-2005_08
ORD IDord-bd9d4db4d73548c3a39c7e8279000e13
Source noteuspto-grants-2005_08