Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 4-Chlorobenzyl alcohol | HCID 13397 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl 4-(bromomethyl)benzoate | HCID 256687 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67007991 | HCID 67007991 | — |
Reaction Steps
To a solution of 4-chlorobenzyl alcohol (4.10 g) in N,N-dimethylformamide (110 ml), sodium hydride (60 to 72%, 952 mg) was added in an ice bath, and the mixed solution was stirred for 30 min. Then, to the resulting solution, 4-(bromomethyl)benzoic acid methyl ester (5.00 g) was added, and the mixed solution was stirred at room temperature for three hours. To the resulting solution, ethyl acetate was added. The resulting solution was washed with water and with a saturated saline solution, sequentially, dried over anhydrous sodium sulfate, and evaporated under reduced pressure to remove the solvent. The resulting crude product was purified by column chromatography (neutral OH type silica gel, ethyl acetate/n-hexane=5 to 9%) to give methyl 4-{[2-(4-chlorophenyl)ethoxy]methyl}benzoate (5.25 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08461329B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-8775549d8f1f48c985d72d651a4e71f8 |
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| Source note | uspto-grants-2013_06 |
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