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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 365591Generated: October 26, 2026

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

https://huagongshe.com/reaction/365591

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 the 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 numberUS06127404
Source datasetuspto-grants-2000_10
ORD IDord-42b9ca8e7fcf4ca8a4f1529ff6bb0fbd
Source noteuspto-grants-2000_10