HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354713Generated: October 27, 2026
Triethylamine → alpha,epsilon-dicarbobenzoxy-L-lysyl-L-phenylalanine benzyl ester
https://huagongshe.com/reaction/354713
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | p-Toluenesulfonate | HCID 85570 | — |
| Reactant | Benzyl 3-phenyl-L-alaninate | HCID 736312 | — |
| Reactant | alpha,epsilon-dicarbobenzoxy-L-lysine | HCID 22822836 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | alpha,epsilon-dicarbobenzoxy-L-lysyl-L-phenylalanine benzyl ester | HCID 22822837 | — |
Reaction Steps
To a stirred solution of α,ε-dicarbobenzoxy-L-lysine (4) (96 mmol, 39.69 g), toluene (310 ml) and triethylamine (96 mmol, 9.70 g) at 0° C., was added, over a period of 15 minutes, iso-butyl chloroformate (109 mmol, 14.88 g), maintaining the temperature between -5° and 0° C. The resulting jelly-like reaction mixture was stirred for 30 minutes at 0° C. and then a slurry of L-phenylalanine benzyl ester, p-toluene sulphonate (1) (96 mmol, 40.99 g) in chloroform (470 ml) and triethylamine (96 mmol, 9.70 g) was added quickly in one portion and the clear solution was allowed to stir at ambient temperature overnight.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04376766 |
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| Source dataset | uspto-grants-1983_03 |
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| ORD ID | ord-ac60421b493c45569276741815aa824e |
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| Source note | uspto-grants-1983_03 |
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