HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 853139Generated: October 26, 2026
Lithium Hydroxide → HCID 86593773, compound
https://huagongshe.com/reaction/853139
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Ethyl (2E)-4-oxo-4-phenyl-2-butenoate | HCID 5369605 | — |
| Reactant | L-Lysine, N6-(trifluoroacetyl)- | HCID 7009573 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86593773 | HCID 86593773 | 191% |
Reaction Steps
To 100 ml of ethanol were added 9.69 g of N6-trifluoroacetyl-L-lysine and 8.16 g of trans-ethyl β-benzoylacrylate. Thereto was added 40 ml of 1N aqueous solution of lithium hydroxide over about 2 hours with stirring, while maintaining the temperature at about −5° C., and the stirring was further continued for 30 minutes. The reaction was terminated by adding 10 ml of concentrated hydrochloric acid thereto. To the reaction mixture were added 130 ml of ethanol and 5 g of 10% palladium-carbon, and a reduction reaction was carried out at about 40° C. under ordinary pressure. After the reaction, the catalyst was removed by suction filtration. The obtained ethanol solution was adjusted to about pH 4 with sodium hydroxide, added with water and concentrated under reduced pressure to distil away ethanol so as to replace the solvent with water. The resulting crystals were filtered with suction and dried under vacuum to give 33 g of N2-(1-ethoxycarbonyl-3-phenylpropyl)-N6-trifluoroacetyl-L-lysine (1S/1R ratio =80/20).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07253299B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-cf569b3f9e43473dbcc7cf40ce74caa1 |
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| Source note | uspto-grants-2007_08 |
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