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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415957Generated: October 30, 2026

Ethyl propiolate → HCID 178448514, compound

https://huagongshe.com/reaction/415957

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl propiolateHCID 12182—
Reactanttert-Butylhydrazine monohydrochlorideHCID 81889—
ReactantPotassium tert-butoxideHCID 23665647—
Solventtert-ButanolHCID 6386—
ProductHCID 178448514HCID 1784485141.1%

Reaction Conditions

Temperature35 °C

Reaction Steps

t-Butylhydrazine hydrochloride (4.5 g, 35.7 mmol) was suspended in t-butanol (35 ml) at room temperature in a dry nitrogen atmosphere. The mixture was warmed to 35° C., ethyl propiolate (3.85 g, 39.3 mmol) dropwise added and, after ice cooling, potassium t-butoxide (13.8 g, 107 mmol) was slowly added in small portions. The resulting mixture was stirred overnight at room temperature. The solvent was evaporated in vacuo, water added to the residue and extracted with dichloromethane. The aqueous phase was acidified by addition of acetic acid, evaporated to dryness in vacuo and the residue was extracted several times with ethyl acetate. The combined organic phases were dried over sodium sulphate, filtered and evaporated yielding 53 mg of 1-tert-butyl-1H-pyrazol-3-ol as a beige colour solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088812B2
Source datasetuspto-grants-2012_01
ORD IDord-8459ea08eb6f4f1f91fc499812ef8ce5
Source noteuspto-grants-2012_01