HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1297543Generated: October 30, 2026
1,3-Dimethoxybenzene → 1,3-Dimethoxy-2-(4-ethylbenzyl)benzene
https://huagongshe.com/reaction/1297543
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,3-Dimethoxybenzene | HCID 9025 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1-(Bromomethyl)-4-ethylbenzene | HCID 12231560 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1,3-Dimethoxy-2-(4-ethylbenzyl)benzene | HCID 23072732 | 49.7% |
Reaction Steps
To a mixture of 1,3-dimethoxybenzene (6.9 g, 50 mmol) and tetrahydrofuran (70 mL), n-butyllithium (1.57 M in hexane, 35 mL) was added in ice and stirred for 1.5 hours. Subsequently, 4-ethylbenzyl bromide (10 g, 50 mmol) was added in ice and stirred for an additional 3.5 hours. 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=95:5–85:15) to give 1,3-dimethoxy-2-(4-ethylbenzyl)benzene (6.37 g, 49%, mp 62.5–66.5° C.) as a light-yellow powder.
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-5e1f239e86fa409c985ddaa735520dc9 |
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| Source note | uspto-grants-2007_07 |
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