HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1681980Generated: November 2, 2026
HCID 13817964, compound → N-formyl-(S)-leucine (S)-1-[[(2S,3S)-3-ethyl-4-oxo-2oxetanyl]methyl]octadecyl ester
https://huagongshe.com/reaction/1681980
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 13817964 | HCID 13817964 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-formyl-(S)-leucine (S)-1-[[(2S,3S)-3-ethyl-4-oxo-2oxetanyl]methyl]octadecyl ester | HCID 13817968 | — |
Reaction Steps
565 mg of N-[(benzyloxy)carbonyl]-L-leucine (S)-1-[[(2S,3S)-3-ethyl-4-oxo-2-oxetanyl]methyl]octadecyl ester were dissolved in 12 ml of THF. The mixture was hydrogenated at room temperature in the presence of 40 mg of 10% Pd/C. After the reaction was finished the catalyst was filtered off and the filtrate was evaporated. The residue was taken up in 9 ml of THF and 71 μl of formic acid/acetic acid anhydride were added dropwise. The mixture was diluted with 5 ml of diethyl ether and washed twice with 2% sodium hydrogen carbonate solution and then with water. After drying over sodium sulfate it was filtered and evaporated. By chromatography on silica gel and recrystallization from n-pentane there was obtained N-formyl-(S)-leucine (S)-1-[[(2S,3S)-3-ethyl-4-oxo-2oxetanyl]methyl]octadecyl ester of m.p. 60°-61° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05175186 |
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| Source dataset | uspto-grants-1992_12 |
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| ORD ID | ord-29cf7547d91743c19ca2a9ed5b7df2ab |
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| Source note | uspto-grants-1992_12 |
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