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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158456Generated: November 2, 2026

N-bromobutanimide → 1-Bromo-4-methoxy-5-(3-methoxy-propoxy)-2-methyl-benzene

https://huagongshe.com/reaction/1158456

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2-Methoxy-1-(3-methoxy-propoxy)4-methyl-benzeneHCID 57790758—
SolventAcetonitrileHCID 6342—
Product1-Bromo-4-methoxy-5-(3-methoxy-propoxy)-2-methyl-benzeneHCID 59223954—

Reaction Steps

To a solution of 2-methoxy-1-(3-methoxy-propoxy)-4-methyl-benzene (2.00 g, 9.51 mmol) in MeCN (30 mL) is added N-bromosuccinimide (1.96 g, 10.5 mmol) at room temperature. Stirring is continued for 2 hrs, followed by evaporation of the solvent. The title compound is obtained after flash chromatography on silica gel (hexane/AcOEt 6:1) as an oil. MS: 289.0/291.0 [M]+. tR (HPLC, Nucleosil C18HD column, 20-100% CH3CN/H2O/6 min, 100% CH3CN/2 min, CH3CN and H2O containing 0.1% TFA, flow: 1 mL/min): 5.04 min. 1H-NMR (CDCl3): δ 2.13 (m, 2H), 2.36 (s, 3H), 3.39 (s, 3H), 3.58 (m, 2H), 3.87 (s, 3H), 4.12 (m, 2H), 6.77 (s,1H), 7.08 (s, 1H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807709B2
Source datasetuspto-grants-2010_10
ORD IDord-61fd5f747cda4ceb8476ce3e741b326a
Source noteuspto-grants-2010_10