HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 236044Generated: October 25, 2026
L-Phenylalanine, methyl ester → L-Phenylalanine, L-alpha-aspartyl-, 2-methyl ester, hydrochloride (1:1)
https://huagongshe.com/reaction/236044
Participants
| Role | Name | HCID | Charge |
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| Reactant | L-Phenylalanine, methyl ester | HCID 736234 | — |
| Reactant | Chloroacetyl l-aspartic acid anhydride | HCID 53642311 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | L-Phenylalanine, L-alpha-aspartyl-, 2-methyl ester, hydrochloride (1:1) | HCID 134600 | 48% |
Reaction Steps
150 Grams of N-chloroacetyl-L-aspartic acid anhydride are quickly added, at -5° C., to the solution of 140 grams of methyl L-phenylalaninate in 400 ml of dichloroethane plus 200 ml of acetic acid. The mixture is stirred for 1 hour at -5° C.; the temperature is then raised, in 2 hours, to 15° C., then, in 30 minutes, to 40° C. The dichloroethane is evaporated under vacuum; 500 ml of methanol and 60 grams of thiourea are added and the mixture is refluxed for 3 hours. After cooling to 20° C., 200 ml of methanol, containing 11% (by weight) of HCl, are added, the solution is cooled to 0° C. for 1 hour, filtered and evaporated to dryness in vacuo. The residue is crystallized from 600 ml of water containing 70 g of NaCl: a very pure aspartame hydrochloride is obtained, in a 48% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04642367 |
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| Source dataset | uspto-grants-1987_02 |
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| ORD ID | ord-47bb1c994bc54a1096b3d379686c6f2f |
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| Source note | uspto-grants-1987_02 |
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