HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111842Generated: October 26, 2026
Calcium Acetate → N-benzyloxycarbonyl (beta-benzyl)-L-aspartyl-L-phenylalanine methyl ester
https://huagongshe.com/reaction/1111842
Participants
| Role | Name | HCID | Charge |
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| Reactant | Calcium Acetate | HCID 6116 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | L-Phenylalanine, methyl ester | HCID 736234 | — |
| Reactant | N-benzyloxycarbonyl-(beta-benzyl)-D,L-aspartic acid | HCID 18324139 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-benzyloxycarbonyl (beta-benzyl)-L-aspartyl-L-phenylalanine methyl ester | HCID 14876780 | 79.3% |
Reaction Steps
A 100 mg amount of Thermoase and 100 mg of an inhibitor for proteolytic enzyme obtained from the potato were admixed with 10 ml of tris-hydrochloric acid buffer solution (pH 8.0) containing 2.0 × 10-2M of calcium acetate. The mixture was stirred at 30° C. for 10 minutes. The insoluble material was removed by filtering the solution through a glass filter (G-3). The filtrate was mixed with 715 mg (2.00 mmol) of N-benzyloxycarbonyl-(β-benzyl)-D,L-aspartic acid and 215 mg (1.00 mmol) of L-phenylalanine methyl ester and then 1N NaOH was added to the filtrate to adjust the pH to 7.5. The reaction was carried out with stirring at 39° C. for 17 hours. The resulting white precipitate was treated in accordance with the process of Example 1 whereby 411 mg (yield of 79.2%) of N-benzyloxycarbonyl-(β-benzyl)-L-aspartyl-L-phenylalanine methyl ester having an [α]D23 = -12.5 (C=1.0 dimethylformamide)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04119493 |
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| Source dataset | uspto-grants-1978_10 |
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| ORD ID | ord-554eda8bc5b542fe905b0a2b250d8169 |
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| Source note | uspto-grants-1978_10 |
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