HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723915Generated: October 30, 2026
5-Bromo-1,2,3-trimethoxybenzene → HCID 86589618, compound
https://huagongshe.com/reaction/1723915
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Bromo-1,2,3-trimethoxybenzene | HCID 75885 | — |
| Reactant | HCID 86589619 | HCID 86589619 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 86589618 | HCID 86589618 | 73.1% |
Reaction Steps
A solution 5-bromo-1,2,3-trimethoxy-benzene (276 mg, 1.12 mmol) dissolved in 6 mL anhydrous ether is cooled to −78° C. and tert-butyllithium (1.7 M in pentane, 1.32 mL, 2.24 mmol) is added. The mixture was stirred at −78° C. for 15 minutes, then at room temperature for 3 hours. Aldehyde 241 (100 mg, 0.373 mmol) was added dropwise over 10 minutes in 10 mL ether at −30° C. The mixture was stirred for 0.5 hours and the reaction quenched with dropwise addition of saturated aqueous NH4+Cl−. The phases were separated and the aqueous phase was extracted with ether (4×10 mL). The pooled organic extracts were washed with saturated aqueous NaHCO3, brine, dried (MgSO4), filtered and concentrated under vacuum. The residue was purified by flash chromatography over silica gel (25% ethyl acetate-hexanes) to yield 243(119 mg, 73%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07485660B2 |
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| Source dataset | uspto-grants-2009_02 |
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| ORD ID | ord-65efa050da80417a996faae23cd72a2c |
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| Source note | uspto-grants-2009_02 |
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