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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 457534Generated: October 30, 2026

Water → 3-Bromo-5-methoxymethoxy-benzaldehyde

https://huagongshe.com/reaction/457534

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethylformamideHCID 6228—
Reactant1,3-Dibromo-5-(methoxymethoxy)benzeneHCID 19261580—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
Product3-Bromo-5-methoxymethoxy-benzaldehydeHCID 1926159574%

Reaction Steps

n-BuLi (8.34 mL of a 1.6 M solution in Et2O, 13.34 mmol) was added dropwise to a solution cooled to −78° C. of 1,3-dibromo-5-methoxymethoxy-benzene (3.59 g, 12.13 mmol) in anhydrous Et2O (40 mL) under a nitrogen atmosphere. The solution was aged at −78° C. for 45 m, anhydrous DMF (1.03 mL, 13.34 mmol) was added, and the reaction mixture was slowly warmed to RT. The mixture was poured into H2O (50 mL), and the aqueous phase was extracted with Et2O (2×75 mL). The combined organic fractions were washed with brine (50 mL) and dried over anhydrous MgSO4. The solvents were evaporated, and the remaining oil was purified by flash chromatography over silica gel (0% to 10% EtOAc/hexanes) to afford 2.18 g (74%) of 3-bromo-5-methoxymethoxy-benzaldehyde (113b).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07189718B2
Source datasetuspto-grants-2007_03
ORD IDord-5d941e1dba994ae9b812599144400742
Source noteuspto-grants-2007_03