HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 47705Generated: October 23, 2026
Water → ethyl (2R)-2-(acetylamino)-3-(3-nitrophenyl)propanoate
https://huagongshe.com/en/reaction/47705
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ammonium Bicarbonate | HCID 14013 | — |
| Reactant | Ethyl 2-(acetylamino)-3-(3-nitrophenyl)propanoate | HCID 22292739 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | ethyl (2R)-2-(acetylamino)-3-(3-nitrophenyl)propanoate | HCID 86584419 | 50% |
Reaction Steps
A mixture of 2.8 g of ethyl 2-(acetylamino)-3-(3-nitrophenyl)propanoate in 17 cm3 of acetonitrile [lacuna] to which is added 3.95 g of ammonium hydrogen carbonate and 35 cm3 of water at a pH in the region of 8. 0.017 g of type-II α-chymotrypsin is then introduced and the mixture is left stirring at room temperature for 1 hour 15 min, while measuring the pH regularly. After this reaction time, the pH is less than 8, a further 0.017 g of type-II α-chymotrypsin is added and stirring of the reaction medium is continued for 2 hours 45 min. The aqueous phase is extracted with 3 times 50 cm3 of ethyl acetate; the combined organic phases are then dried over sodium sulfate, filtered and evaporated under reduced pressure (2 kPa) at a temperature in the region of 40° C. 1.4 g of ethyl (2R)-2-(acetylamino)-3-(3-nitrophenyl)propanoate are obtained in the form of white crystals melting at 110° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06699895B2 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-ae19ad4a9f554c3ebcf9eb8e690ab98e |
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| Source note | uspto-grants-2004_03 |
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