HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5751Generated: October 25, 2026
Triethylamine → BOC-p-nitrophenylalanine 2-oxopropyl amide
https://huagongshe.com/reaction/5751
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 2-Propanone, 1-amino-, hydrochloride | HCID 3084025 | — |
| Reactant | N-(tert-Butoxycarbonyl)-4-nitro-L-phenylalanine | HCID 7021882 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | BOC-p-nitrophenylalanine 2-oxopropyl amide | HCID 18632424 | — |
Reaction Steps
t-Butyloxycarbonyl-p-nitrophenylalanine (4.42 g, 14.26 mmol, aminoacetone hydrochloride (1.56 g, 14.26 mmol), triethylamine (1.44 g, 14.26 mmol), 1-hydroxybenzotriazole (1.69 g, 12.55 mmol), were dissolved in ethyl acetate (400 ml). 1,3-Dicyclohexylcarbodiimide (3.23 g, 15.68 mmol) in ethyl acetate (25 ml) was added and the solution allowed to stir for 18 hours. Glacial acetic acid (0.2 ml) was added and the solution was filtered. The filtrate was extracted with saturated salt solution (100 ml), 1N HCl solution (3×100 ml), saturated salt solution (100 ml), 5% bicarbonate solution (3×100 ml), and saturated salt solution (100 ml). The organic phase was dried over MgSO4, filtered and concentrated to 50 ml. Petroleum ether (50 ml) was added and the solution was cooled to 0° C. for 12 hours. The precipitated product was collected and dried under vacuum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05246692 |
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| Source dataset | uspto-grants-1993_09 |
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| ORD ID | ord-777c1fb9b65b4cdf9d3f220923205cdd |
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| Source note | uspto-grants-1993_09 |
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