HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 993339Generated: October 29, 2026
Water → Benzyl N,N-dibenzyl-L-phenylalaninate
https://huagongshe.com/reaction/993339
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | L-Phenylalanine | HCID 6140 | — |
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Benzyl N,N-dibenzyl-L-phenylalaninate | HCID 10928230 | — |
Reaction Steps
A solution containing L-phenylalanine (161 kg, 975 moles), potassium carbonate (445 kg, 3220 moles), water (675 L), ethanol (340 L), and benzyl chloride (415 kg, 3275 moles) was heated to 90±15° C. for 10-24 hours. The reaction mixture was cooled to 60° C. and the lower aqueous layer was removed. Heptane (850 L) and water (385 L) were added to the organics, stirred, and the layers separated. The organics were then washed once with a water/methanol mixture (150 L/150 L). The organics were then stripped to give the desired product as an oil, which was carried on in the next step without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06472529B2 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-6783f91f7ac746f089ea88053a7fe88c |
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| Source note | uspto-grants-2002_10 |
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