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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 743379Generated: October 27, 2026

Benzenemethanol, 2-(phenylmethoxy)- → 1-(Benzyloxy)-2-(chloromethyl)benzene

https://huagongshe.com/reaction/743379

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenemethanol, 2-(phenylmethoxy)-HCID 18811—
ReactantThionyl ChlorideHCID 24386—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product1-(Benzyloxy)-2-(chloromethyl)benzeneHCID 563507—

Reaction Steps

The whole of the 2-benzyloxybenzyl alcohol thus obtained was dissolved in 500 ml of tetrahydrofuran, and 85 ml of thionyl chloride were added dropwise, whilst ice-cooling, to the resulting solution. The reaction mixture was then allowed to stand overnight at room temperature, after which it was concentrated by evaporation under reduced pressure to give a dark colored oil. This product was dissolved in toluene, and the solution was decolorized by treating it with silica gel for chromatography followed by filtration. The filtrate was concentrated by evaporation under reduced pressure to give 2-benzyloxybenzyl chloride as a yellow oil, which was used in the following reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05556864
Source datasetuspto-grants-1996_09
ORD IDord-de01410fa79f49dd8e2a4f0cc6602f7b
Source noteuspto-grants-1996_09