HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1036737Generated: October 25, 2026
Water → (R)-2-(2-(tert-Butoxycarbonylamino)-2-methylpropanamido)-4-phenylbutanoic acid
https://huagongshe.com/reaction/1036737
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | D-Homophenylalanine | HCID 6950302 | — |
| Reactant | Tert-butyl 1-(2,5-dioxopyrrolidin-1-yl)-2-methyl-1-oxopropan-2-ylcarbamate | HCID 71060486 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (R)-2-(2-(tert-Butoxycarbonylamino)-2-methylpropanamido)-4-phenylbutanoic acid | HCID 22862434 | — |
Reaction Steps
A mixture comprising of tert-Butyl 1-(2,5-dioxopyrrolidin-1-yl)-2-methyl-1-oxopropan-2-ylcarbamate (1 g, 3.52 mmol) (prepared according to the procedure described in EP1486498A1 page 20) and H-D-Homophe-OH (0.630 g, 3.52 mmol) in THF (16 ml)/water (4 ml) was treated with triethylamine (1.471 ml, 10.55 mmol). The reaction mixture was stirred at 50° C. for 9 hours. THF was removed in vacuo. The aqueous solution was further diluted with water and the pH adjusted to pH 2-3 using 1M HCl. The resulting aqueous phase was extracted with EtOAc. The organic portion was dried (MgSO4) and concentrated in vacuo to afford the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08546416B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-dc4a3cf71c9c482baed69d543722a3d6 |
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| Source note | uspto-grants-2013_10 |
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