HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604745Generated: October 30, 2026
1-Bromo-4-ethylbenzene → α-(4-Ethylphenyl)-2-(phenylmethoxy)benzenemethanol
https://huagongshe.com/reaction/604745
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromo-4-ethylbenzene | HCID 15313 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-(Benzyloxy)benzaldehyde | HCID 344784 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Catalyst | 1-Bromo-4-ethylbenzene | HCID 15313 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | α-(4-Ethylphenyl)-2-(phenylmethoxy)benzenemethanol | HCID 67069123 | 101.4% |
Reaction Steps
1-Bromo-4-ethylbenzene (6.69 g, 0.036 mol) was added to a suspension of magnesium (17.2 g) and tetrahydrofuran (50 mL) and heated to reflux. Subsequently, a tetrahydrofuran (300 mL) solution of 1-bromo-4-ethylbenzene (97.9 g, 0.529 mol) was added for two hours at room temperature. After stirred at room temperature for 1.5 hours, the reaction mixture was cooled to 4° C. and a tetrahydrofuran (100 mL) solution of 2-benzyloxybenzaldehyde (100 g, 0.471 mol) was added for one hour. After stirred for two hours, the reaction mixture was poured into a saturated ammonium chloride aqueous solution. After the mixture was extracted with ethyl acetate, the organic phase was washed with brine and then dried with anhydrous magnesium sulfate. After the desiccant was filtered off, the residue obtained by evaporating the solvent under reduced pressure was purified by silica gel column chromatography (hexane:ethyl acetate=95:5) to obtain (2-benzyloxyphenyl)(4-ethylphenyl)methanol (152 g) as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07910619B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-504a6e10b67a44f99bff5e160191ec8b |
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| Source note | uspto-grants-2011_03 |
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