HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131052Generated: October 25, 2026
Triethylamine → Ethyl 2-(4-nitrophenylamino)-3-methylbutyrate
https://huagongshe.com/reaction/131052
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | p-Fluoronitrobenzene | HCID 9590 | — |
| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | l-Valine, ethyl ester | HCID 87182 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 2-(4-nitrophenylamino)-3-methylbutyrate | HCID 58596142 | 32.7% |
Reaction Steps
162 mg of 4-fluoronitrobenzene, 200 mg of L-valine ethyl ester and 0.4 ml of Et3N were added to a solution of 10 ml of N-methylpyrrolidinone (NMP). The reaction medium was heated at 70° C. for 8 hours and, after cooling to room temperature, then poured into a water and ice mixture. The yellow precipitate formed was filtered off, re-slurried in water and then dried over P2O5. 100 mg of ethyl 2-(4-nitrophenylamino)-3-methylbutyrate (8) were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07384432B2 |
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| Source dataset | uspto-grants-2008_06 |
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| ORD ID | ord-a406a4bad6cf4634999741d2ef7864de |
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| Source note | uspto-grants-2008_06 |
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