HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354283Generated: November 1, 2026
Water → 1-(2-(Benzyloxy)ethyl)-4-bromobenzene
https://huagongshe.com/reaction/2354283
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-(4-Bromophenyl)ethanol | HCID 72851 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(2-(Benzyloxy)ethyl)-4-bromobenzene | HCID 21909303 | — |
Reaction Steps
To a solution of 2-(4-bromophenyl)ethanol (1.0 g) in N,N-dimethylformamide (25 mL) was added 55% sodium hydride (0.26 g) under ice-cooling, and the mixture was stirred at the same temperature for 15 minutes. To this mixture was added benzyl bromide (0.77 mL) at the same temperature, and the mixture was stirred at the same temperature for 15 minutes, and stirred at room temperature for 30 minutes. The reaction mixture was poured into water, and the resulting mixture was extracted with diethyl ether. The extract was washed with water and brine successively, and dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure, and the residue was purified by column chromatography on silica gel (eluent: n-hexane-n-hexane/ethyl acetate=20/1) to give 1-[2-(benzyloxy)ethyl]-4-bromobenzene (1.35 g). The title compound was prepared in a similar manner to that described in Step 2 of Reference Example 46 using this material instead of 1-bromo-2-fluoro-4-methoxybenzene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07750145B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-d0dec30b08504739b6e24d7b594fbbf0 |
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| Source note | uspto-grants-2010_07 |
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