HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 901038Generated: October 30, 2026
Ethyl iodoacetate → ethyl 2-(3-amino-1H-pyrazol-1-yl)acetate
https://huagongshe.com/reaction/901038
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl iodoacetate | HCID 12183 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 178418806 | HCID 178418806 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | ethyl 2-(3-amino-1H-pyrazol-1-yl)acetate | HCID 5200378 | — |
Reaction Steps
57.1 To a stirred, cooled (0° C.) solution of the 1.6 g 3-aminopyrazole in DMF under an argon atmosphere was added potassium tert-butylate. After 30 min. stirring at 0° C., ethyl iodoacetate was added in one portion. After 2 h stirring at 0° C., the ice bath was removed and stirring at r.t. was continued for 22 h. The mixture was concentrated in order to remove as much DMF as possible. The residue was taken up in EtOAc and washed with H2O. The aqueous phase was extracted with EtOAc. The combined organics were washed with H2O and brine, dried (MgSO4), filtered and concentrated. The crude product was purified by chromatography on silica using a gradient from cyclohexane to EtOAc in 40 min to give 366 mg (3-amino-pyrazol-1-yl)-acetic acid ethyl ester as viscous yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07361672B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-3fe3b0ef5c0e414da7441f2ba5addd19 |
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| Source note | uspto-grants-2008_04 |
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