HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485118Generated: November 2, 2026
Sodium hydride → Ethyl N-(5-phenylpentyl)-beta-alaninate
https://huagongshe.com/reaction/1485118
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | (5-Bromopentyl)benzene | HCID 285561 | — |
| Reactant | HCID 131736734 | HCID 131736734 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl N-(5-phenylpentyl)-beta-alaninate | HCID 118113289 | — |
Reaction Steps
To a solution of β-alanine ethyl hydrochloride (2.00 g) in N,N-dimethylformamide (65.0 mL), sodium hydride (60% dispersion in mineral oil, 1.15 g) was added and the mixture was stirred at room temperature for an hour. After adding (5-bromopentyl)benzene (2.52 mL), the mixture was stirred at 80° C. for 4 hours. After being cooled to room temperature, the reaction mixture was diluted with ethyl acetate and washed with saturated brine. The organic layer was separated off and dried over anhydrous magnesium sulfate; after removing the desiccant by filtration, the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (chloroform:methanol=100:0-85:15) to give the titled compound as a pale yellow oil (480 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09422240B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-5726010410a04f0a92b5dd881db6b806 |
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| Source note | uspto-grants-2016_08 |
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