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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium HydroxideHCID 14798—
ReactantL-NorvalineHCID 65098—
SolventWaterHCID 962—
Product(S)-benzyl 2-(dibenzylamino)pentanoateHCID 44223288132.9%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143448B2
Source datasetuspto-grants-2012_03
ORD IDord-3dcbdde81e2d4c52b94f18c81193f062
Source noteuspto-grants-2012_03