HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588863Generated: October 26, 2026
Allyl Alcohol → 3-(5-Bromo-4-chloro-2-methoxyphenyl)propanal
https://huagongshe.com/reaction/588863
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allyl Alcohol | HCID 7858 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-Bromo-2-chloro-5-iodo-4-methoxybenzene | HCID 90455719 | — |
| Catalyst | Tetrabutylammonium Chloride | HCID 70681 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(5-Bromo-4-chloro-2-methoxyphenyl)propanal | HCID 117607187 | 34% |
Reaction Steps
A mixture of 1-bromo-2-chloro-5-iodo-4-methoxybenzene (3.2 g, 9.2 mmol), prop-2-en-1-ol (1.3 g, 23.0 mmol), Pd(OAc)2 (206 mg, 0.9 mmol), TBAC (2.56 g, 9.2 mmol), NaHCO3 (2.3 g, 27.6 mmol) in DMF (50 mL) was stirred under Argon at 60° C. for 16 h. The mixture was allowed to cool to RT, and then partitioned between ethyl acetate and water. The combined organic layer was washed with brine, dried over anhydrous Na2SO4 and concentrated. The residue was purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=1:20) to afford the desired product (860 mg, 34% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09227978B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-199a28c7717345d09e3da49099e2d18d |
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| Source note | uspto-grants-2016_01 |
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