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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748757Generated: October 30, 2026

Trifluoroacetic acid → HCID 86724100, compound

https://huagongshe.com/reaction/1748757

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantEthyl orthoformateHCID 31214—
ReactantHCID 86724099HCID 86724099—
SolventDichloromethaneHCID 6344—
ProductHCID 86724100HCID 86724100—

Reaction Steps

To a solution of 1-methyl-5-nitro-1H-pyrazole-3-carbohydrazide (3.81 g, 20.6 mmol) in DCM (30 mL) was added 2,2,2-trifluoroacetic acid (4 mL, 51.9 mmol). The mixture was stirred for about 2 h then concentrated under reduced pressure. To the residue was added triethoxymethane (31.4 mL, 206 mmol) and the mixture was refluxed for about 24 h. The reaction was cooled to ambient temperature and continued to stir for about 16 h. The reaction mixture was concentrated under reduced pressure and the material was partitioned between DCM (25 mL) and saturated NaHCO3 (10 mL). The organic layer was separated and the aqueous layer was back extracted with DCM (25 mL). The combined organic layers were washed with brine (10 mL), dried over MgSO4, filtered and concentrated under reduced pressure and triturated with ether (2×30 mL).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150592B2
Source datasetuspto-grants-2015_10
ORD IDord-c7e0537a03454d5392759c30eba8c6d3
Source noteuspto-grants-2015_10