HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 261318Generated: October 25, 2026
L-Phenylalanine, methyl ester → L-Phenylalanine, methyl ester
https://huagongshe.com/reaction/261318
Participants
| Role | Name | HCID | Charge |
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| Reactant | L-Phenylalanine, methyl ester | HCID 736234 | — |
| Reactant | N-(Benzyloxycarbonyl)aspartic acid | HCID 2723942 | — |
| Product | L-Phenylalanine, methyl ester | HCID 736234 | 95.5% |
| Product | N-(Benzyloxycarbonyl)-L-aspartyl-L-phenylalanine methyl ester | HCID 10159630 | — |
Reaction Steps
A 267.2 mg (1 m mol) of N-benzyloxycarbonyl-L-aspartic acid and 537.6 mg (3 m mol) of L-phenylalanine methyl ester were dissolved in 5 ml of McIlvain's buffer solution (pH:7.0). The resulting solution was admixed with 100 mg of Thermoase and 100 mg of potato inhibitor and shaken at 38° C. for 20 hours. The precipitate was collected and washed with water and dried to obtain 580 mg of a crude crystalline addition compound of N-benzyloxycarbonyl-L-aspartyl-L-phenylalanine methyl ester and L-phenylalanine methyl ester (1:1) (melting point: 123 to 125° C.; Yield: 95.5 % based on N-benzyloxycarbonyl-L-aspartic acid).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04165311 |
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| Source dataset | uspto-grants-1979_08 |
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| ORD ID | ord-a6ac13c602844c159491d47fe00fb0a2 |
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| Source note | uspto-grants-1979_08 |
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