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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1026902Generated: November 1, 2026

Ethanol → HCID 178469973, compound

https://huagongshe.com/reaction/1026902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantTriethylamineHCID 8471—
ReactantTrimethylsilyl triflateHCID 65367—
Reactant3-(2,2-Dimethyl-4,6-dioxo-1,3-dioxan-5-ylidene)amino-4-carbethoxy-pyrazoleHCID 540759—
SolventDichloromethaneHCID 6344—
ProductHCID 178469973HCID 17846997391.7%

Reaction Steps

Ethyl 5-[(2,2-dimethyl-4,6-dioxo-1,3-dioxane-5-ylidene)methylamino]1H-pyrazole-4-carboxylate (14.9 g, 45.6 mmol) obtained in step 1 was suspended in methylene chloride (227 mL), and triethylamine (25 mL, 182 mmol) was added. Trimethylsilyl trifluoromethanesulfonate (33.2 mL, 182 mmol) was added dropwise over about 10 min under ice-cooling while maintaining the reaction inside temperature at not more than 10° C., and the mixture was stirred at room temperature for 1 hr. The reaction mixture was cooled to 0° C., and ethanol (75 mL) was added dropwise over 10 min. After the completion of the dropwise addition, the mixture was stirred at room temperature for 10 hr. The precipitated crystals were collected by filtration, washed with cold ethanol (50 mL), and dried under reduced pressure at 40° C. overnight to give the title compound (10.5 g, 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729264B2
Source datasetuspto-grants-2014_05
ORD IDord-1e34d2b8456c457f894d0462e08e5c34
Source noteuspto-grants-2014_05