Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 841966Generated: October 26, 2026

Formaldehyde → HCID 12051530, compound

https://huagongshe.com/reaction/841966

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantEthyl chloroformateHCID 10928—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 178470514HCID 178470514—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductHCID 12051530HCID 1205153053%

Reaction Steps

Ethyl 5-(4,5-dimethoxy-2-nitrobenzoyl)-1H-1,2,3-triazole-4-carboxylate (Synthesis Example 2) (70 mg) and p-toluenesulfonic acid monohydrate (17 mg) were suspended in methylene chloride (10 ml) under an argon atmosphere. Paraformaldehyde (6 mg) was added thereto. The mixture was stirred at room temperature for 30 min. Pyridine (0.05 ml) and ethyl chloroformate (0.04 ml) were added thereto, and the mixture was stirred at room temperature for one hr. Further, pyridine (0.02 ml) and ethyl chloroformate (0.04 ml) were added thereto, and the mixture was stirred for 10 min. The solvent was evaporated under reduced pressure. Ethyl acetate (15 ml) and a saturated aqueous sodium hydrogencarbonate solution (10 ml) were added thereto, followed by separation. The organic layer was washed with a saturated aqueous sodium hydrogencarbonate solution (10 ml) and saturated brine solution (10 ml) in that order and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to give ethyl 2-(ethoxycarbonyloxymethyl)-5-(4,5-dimethoxy-2-nitrobenzoyl)-2H-1,2,3-triazole-4-carboxylate as a light yellow foam (48 mg, 53%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06372735B1
Source datasetuspto-grants-2002_04
ORD IDord-431e17caab6848c1b670e4d40019565e
Source noteuspto-grants-2002_04