HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2360591Generated: October 26, 2026
Water → 1-(2-Bromoethyl)-4-(methoxymethyl)benzene
https://huagongshe.com/reaction/2360591
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | [4-(2-Bromoethyl)phenyl]methanol | HCID 22337010 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(2-Bromoethyl)-4-(methoxymethyl)benzene | HCID 20197428 | 65.1% |
Reaction Steps
To a suspension of 60% NaH in paraffin (13.9 mmol; 0.56 g) in THF (20 ml) cooled to 0° C. was first added, dropwise, a solution of 4-(2-bromoethyl)benzyl alcohol (9.25 mmol; 1.99 g) in THF (20 ml) in an ice bath, followed by iodomethane (13.9 mmol; 1.972 g; 0.86 ml). The mixture was stirred at room temperature for 1 hour 30 minutes, after which it was poured into water and extracted with ethyl acetate. The combined organic phases were washed with saturated NaCl solution (3×20 ml), dried over anhydrous sodium sulfate and evaporated under reduced pressure. The residue was chromatographed on a column of alumina, eluting with ethyl acetate, to give 1.38 g of product as an oil (65%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08686147B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-b97585ac876e4579915a94f0d0fadb0f |
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| Source note | uspto-grants-2014_04 |
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