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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 269863Generated: October 26, 2026

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

https://huagongshe.com/reaction/269863

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 numberUS07449455B2
Source datasetuspto-grants-2008_11
ORD IDord-3e45a5c8c33c41d58e211d2d10b555a1
Source noteuspto-grants-2008_11