HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1297541Generated: October 30, 2026
1-Bromo-4-ethylbenzene → HCID 69200004, compound
https://huagongshe.com/reaction/1297541
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromo-4-ethylbenzene | HCID 15313 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Benzoic acid, 3-formyl-4-hydroxy-, methyl ester | HCID 212595 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Reactant | HCID 178506701 | HCID 178506701 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69200004 | HCID 69200004 | 46% |
Reaction Steps
To a mixture of methyl 3-formyl-4-hydroxybenzoate (4.0 g, 22.2 mmol) and tetrahydrofuran (100 mL), 4-ethylphenyllithium [which had been prepared by stirring t-butyllithium (66 mmol) into a mixture of 1-bromo-4-ethylbenzene (12.3 g, 66 mmol) and tetrahydrofuran (200 mL) at −70° C. for 30 minutes] was added at −70° C. and stirred for 1 hour. After addition of saturated aqueous ammonium chloride, the reaction mixture was extracted with ethyl acetate, and the organic phase was washed with saturated aqueous sodium chloride and then dried over anhydrous magnesium sulfate. After the solvent was distilled off under reduced pressure, the resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=65:35–50:50) to give methyl 3-[(4-ethylphenyl)hydroxymethyl]benzoate (2.92 g, 46%) as a light-yellow gum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07250522B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-337b194a351a4e958bb602b58122863d |
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| Source note | uspto-grants-2007_07 |
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