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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 439723Generated: October 25, 2026

Acetic Acid → Ethyl 4,5,6,7-tetrahydro-1,3-dimethyl-4-oxo-1H-indazole-5-carboxylate

https://huagongshe.com/reaction/439723

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium hydrideHCID 24758—
Reactant1,3-dimethyl-4,5,6,7-tetrahydro-1H-indazol-4-oneHCID 14126679—
ReactantCID 21226545HCID 21226545—
SolventBenzeneHCID 241—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductEthyl 4,5,6,7-tetrahydro-1,3-dimethyl-4-oxo-1H-indazole-5-carboxylateHCID 2240293363.9%

Reaction Steps

A suspension of sodium hydride (14.6 g, 0.365 mol, 60% oil dispersion) in dry benzene at 5° to 10° C. is treated with 1,5,6,7-tetrahydro-1,3-dimethyl-4H-indazole-4-one (30.0 g, 0.183 mol). The reaction mixture is treated dropwise with ethyl carbonate (45.0 mL, 0.365 mol) and ethanol (1.0 mL) with cooling, stirred for 11 hours at reflux temperature, cooled to room temperature and treated with acetic acid (24.1 g, 0.400 mol) and water. The phases are separated, the organic phase is set aside and the aqueous phase is extracted with ether. The organic phases are combined, washed with water, dried (Na2SO4) and concentrated in vacuo. The resultant residue is chased twice with toluene, recrystallized from (2:1) methylene chloride:heptane and a second time from 50% tetrahydrofuran:heptane to afford the title product (27.6 g, 63.9%), mp 76.5°-79° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05516751
Source datasetuspto-grants-1996_05
ORD IDord-0bf641b14b6a41eba6c9c8e20592fa95
Source noteuspto-grants-1996_05