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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2410089Generated: October 31, 2026

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

https://huagongshe.com/reaction/2410089

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, 2H, J=8.8 Hz), 6.92 (d, 2H, J=8.6 Hz), 4.68 (s, 2H), 4.08 (t, 2H, J=5.9 Hz), 3.77 (t, 2H, J=6.4 Hz); MS (FAB) 266 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815934B2
Source datasetuspto-grants-2014_08
ORD IDord-08bc76932c33483fa06f7def0ed54475
Source noteuspto-grants-2014_08