HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744021Generated: October 29, 2026
Hydrochloric Acid → 2-Acetylamino-6-methyl-6-nitroheptanoic acid
https://huagongshe.com/reaction/1744021
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Diethyl 2-acetylamino-2-(4-methyl-4-nitropentyl)malonate | HCID 9968068 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Acetylamino-6-methyl-6-nitroheptanoic acid | HCID 9856268 | 72.4% |
Reaction Steps
Diethyl 2-acetylamino-2-(4-methyl-4-nitropentyl)malonate (193.5 g, 558.5 mmol) was dissolved in ethanol (270 ml), and potassium hydroxide (51 g, 781.9 mmol) was dissolved in water (250 ml) and added. The mixture was stirred at 90° C. for 1 h, and potassium hydroxide (51 g, 781.9 mmol) was dissolved in water (250 ml) and added. The mixture was stirred at the same temperature for 2 h. The mixture was cooled to 40° C. and concentrated hydrochloric acid was added to adjust the solution to pH 1.5, which solution was stirred overnight at 80° C. Ethanol was evaporated by concentration under reduced pressure and the residue was ice-cooled. The precipitated crystals were separated, and the obtained slurry was washed with ethyl acetate (200 ml) and dried under reduced pressure to give the objective compound (99.6 g, yield 72%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07012152B2 |
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| Source dataset | uspto-grants-2006_03 |
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| ORD ID | ord-65b6724ca9034f3c87783c0012a80ae2 |
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| Source note | uspto-grants-2006_03 |
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