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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1823808Generated: November 1, 2026

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

https://huagongshe.com/reaction/1823808

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 1) 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 numberUS07041663B2
Source datasetuspto-grants-2006_05
ORD IDord-bf62da2b4f3d4583b55d86c24992daa6
Source noteuspto-grants-2006_05