HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1099507Generated: October 25, 2026
Benzyl Bromide → (S)-benzyl 2-(dibenzylamino)pentanoate
https://huagongshe.com/reaction/1099507
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | L-Norvaline | HCID 65098 | — |
| Solvent | Water | HCID 962 | — |
| Product | (S)-benzyl 2-(dibenzylamino)pentanoate | HCID 44223288 | 132.9% |
Reaction Steps
Sodium hydroxide (0.513 Kg; 12.82 moles) and potassium carbonate (1.77 Kg, 12.82 moles) were dissolved in water (7.5 L) and cooled to 0° C. The resulting solution was treated with (S)-2-aminopentanoic acid (L-norvaline, 0.75 Kg; 6.41 moles) slowly at between 0-5° C. The stirred suspension was heated at 90° C. and benzyl bromide (4.385 Kg, 25.64 moles) was added dropwise. Heating was continued for a further 12 hours at 90° C. The reaction mixture was then cooled to ambient temperature, and extracted with ethyl acetate (2×6 liters). The layers were separated and the aqueous phase extracted twice with ethyl acetate. The combined organic extracts were dried over sodium sulfate, and the solvent removed under reduced pressure to obtain 3.3 Kg of crude (S)-benzyl 2-(dibenzylamino)pentanoate, a compound of formula (3), as a brown oil. This material was used in the next reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08143448B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-3dcbdde81e2d4c52b94f18c81193f062 |
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| Source note | uspto-grants-2012_03 |
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