HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1162857Generated: October 29, 2026
(2-Cyanoethyl)hydrazine → HCID 178440339, compound
https://huagongshe.com/reaction/1162857
Participants
| Role | Name | HCID | Charge |
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| Reactant | (2-Cyanoethyl)hydrazine | HCID 136177 | — |
| Reactant | 4-(2-Ethoxycarbonyl-4-methyl-3-oxo-pentyl)benzoic acid | HCID 58952003 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178440339 | HCID 178440339 | — |
Reaction Steps
15 g of compound 45 are dissolved in 100 ml of glacial acetic acid. 7.4 ml of 2-cyanoethylhydrazine are added, and the solution is heated at 100° C. for 2 h. The mixture is added to ice-water and extracted several times with ethyl acetate. The organic phase is extracted with 20% strength ammonium chloride solution and saturated sodium chloride solution and dried over sodium sulfate. 2.40 g of the desired compound 46 crystallize out with the ethyl acetate phase. The mother liquor is concentrated and chromatographed on silica gel (dichloromethane:methanol:glacial acetic acid=100:10:1). A further 1.10 g of compound 46, plus 7.0 g of reisolated precursor 45, are obtained. C17H19N3O3 (313.4); MS (ESI+): 314.2 (M+H)+, tR=0.97 min (Gradient 2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07820804B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-7edfa9b368dd42f88b58a8ca6cf09f85 |
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| Source note | uspto-grants-2010_10 |
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