HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1733652Generated: October 25, 2026
Chloroform → Ethyl N-(1-((benzyloxy)carbonyl)-L-prolyl)-L-leucinate
https://huagongshe.com/reaction/1733652
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Benzyloxycarbonyl-L-proline | HCID 101987 | — |
| Reactant | L-Leucine, ethyl ester, hydrochloride (1:1) | HCID 11658447 | — |
| Reactant | Ethyl cyano{[(methanesulfonyl)oxy]imino}acetate | HCID 54531055 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | Ethyl N-(1-((benzyloxy)carbonyl)-L-prolyl)-L-leucinate | HCID 6453075 | 40.9% |
Reaction Steps
N-Benzyloxycarbonyl-L-proline (1.25 g) and L-leucine ethyl ester hydrochloride (1.0 g) are suspended into chloroform (10 ml), and therein is dissolved triethylamine (1.40 ml). To the solution is added ethyl 2-methanesulfonyloxyimino-2-cyanoacetate (1.1 g) and the mixture is stirred at room temperature for 16 hours. After reaction, the reaction mixture is extracted with ethyl acetate. The extract is washed with water, 1 N aqueous sodium hydrogen carbonate, water, 1 N hydrochloric acid and water in order and then dried over anhydrous magnesium sulfate. After drying, the solvent is distilled off and the resulting residue is crystallized from petroleum ether to give N-(N-benzyloxycarbonyl-L-prolyl)-L-leucine ethyl ester (0.8 g), melting point: 65°-67° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04242507 |
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| Source dataset | uspto-grants-1980_12 |
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| ORD ID | ord-8efbbd2f237244b7b894d13b45c3f98b |
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| Source note | uspto-grants-1980_12 |
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