HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 457534Generated: October 30, 2026
Water → 3-Bromo-5-methoxymethoxy-benzaldehyde
https://huagongshe.com/reaction/457534
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 1,3-Dibromo-5-(methoxymethoxy)benzene | HCID 19261580 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 3-Bromo-5-methoxymethoxy-benzaldehyde | HCID 19261595 | 74% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07189718B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-5d941e1dba994ae9b812599144400742 |
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| Source note | uspto-grants-2007_03 |
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