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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2237560Generated: November 1, 2026

Ethyl iodoacetate → ethyl 2-(3-amino-1H-pyrazol-1-yl)acetate

https://huagongshe.com/reaction/2237560

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl iodoacetateHCID 12183—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 178418806HCID 178418806—
SolventDimethylformamideHCID 6228—
Productethyl 2-(3-amino-1H-pyrazol-1-yl)acetateHCID 5200378—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07718659B2
Source datasetuspto-grants-2010_05
ORD IDord-b4041f19acc24161a3ed645d032ffb60
Source noteuspto-grants-2010_05