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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 392864Generated: October 29, 2026

N-bromobutanimide → 1-(Benzyloxy)-4-bromo-2-ethyl-5-methoxybenzene

https://huagongshe.com/reaction/392864

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2-(Benzyloxy)-1-ethyl-4-methoxybenzeneHCID 22662099—
SolventCarbon TetrachlorideHCID 5943—
Product1-(Benzyloxy)-4-bromo-2-ethyl-5-methoxybenzeneHCID 22662106—

Reaction Steps

In a bromination reaction, the 3-benzyloxy-4-ethyl-1-methoxybenzene (3) is combined with N-bromosuccinimide (NBS) and silica gel 60 (EM Science, 480 Democrat Road, Gibbstown, N.J. 08027, an affiliate of Merck KGaA, Darmstadt, Germany) in a nonpolar solvent such as carbon tetrachloride at a temperature from about 0° C. to about room temperature. Preferably, the reaction is conducted at about room temperature. This reaction is allowed to stir, in the absence of light, to yield 5-benzyloxy-2-bromo-4-ethyl-1-methoxybenzene (4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06803470B2
Source datasetuspto-grants-2004_10
ORD IDord-5ee50cd272504f13b1988b21ab1465e4
Source noteuspto-grants-2004_10