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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1790389Generated: November 2, 2026

2-(Benzyloxy) ethanol → Benzene, ((2-bromoethoxy)methyl)-

https://huagongshe.com/reaction/1790389

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Benzyloxy) ethanolHCID 12141—
Reactant4-BromopyrazoleHCID 16375—
ReactantSodium hydrideHCID 24758—
SolventTetrahydrofuranHCID 8028—
ProductBenzene, ((2-bromoethoxy)methyl)-HCID 73833—

Reaction Steps

4-Bromopyrazole (2.205 g) was dissolved in tetrahydrofuran (20 ml). Under ice cooling, 60% sodium hydride (625 mg) was added thereto followed by stirring. After 30 min, benzyl 2-bromoethyl ether (3.872 g) obtained from 2-benzyloxyethanol in the same manner as the one of Production Example 1 was added thereto and the resultant mixture was stirred at room temperature overnight. Then the reaction solution was partitioned between ethyl acetate and water and the organic layer was washed with water, dried over magnesium sulfate and concentrated under reduced pressure to give the title compound (2.287 g) as a colorless oil (yield: 53%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07071201B2
Source datasetuspto-grants-2006_07
ORD IDord-e80df2f9f4ce49b5bd2ee745e5f5299b
Source noteuspto-grants-2006_07