HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 554570Generated: October 30, 2026
1-Bromo-4-ethylbenzene → HCID 67459476, compound
https://huagongshe.com/reaction/554570
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Bromo-4-ethylbenzene | HCID 15313 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 3-bromo-4-ethoxybenzaldehyde | HCID 1494336 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67459476 | HCID 67459476 | 88% |
Reaction Steps
THF (10 mL) was added to magnesium (353 mg, 14.5 mmol), and furthermore 1-bromo-4-ethylbenzene (2 mL, 14.5 mmol) was added dropwise thereto and the mixture was heated to reflux for one hour. The reaction mixture was cooled to 0° C., and a solution of 3-bromo-4-ethoxybenzaldehyde (2.21 g, 9.68 mmol) in THF (5 mL) was added thereto and the reaction mixture was stirred at the same temperature for 1.5 hours. To the reaction mixture, a saturated ammonium chloride aqueous solution was added and the resulting mixture was extracted with ethyl acetate. The extract was washed with a saturated sodium chloride aqueous solution and dried over magnesium sulfate. The residue obtained by distilling the solvent under reduced pressure was purified by silica gel column chromatography [developing solution=n-hexane to n-hexane:ethyl acetate (3:1)] to obtain the title compound (2.83 g, 88%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08048897B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-3e789edc0c9e4239b75b4119009ea7ee |
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| Source note | uspto-grants-2011_11 |
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