Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2292663Generated: October 31, 2026

Dimethylformamide → HCID 70150069, compound

https://huagongshe.com/reaction/2292663

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium hydrideHCID 24758—
Reactant1H-1,2,3-TriazoleHCID 67516—
ReactantHCID 21833670HCID 21833670—
ReactantHCID 178418361HCID 178418361—
ProductHCID 70150069HCID 70150069—

Reaction Conditions

Temperature10 °C

Reaction Steps

A mixture of 2H-1,2,3-triazole (2.26 g), sodium hydride (60%, 1.31 g) and anhydrous N,N-dimethylformamide (100 ml) was stirred at 60° to 70° C. under a nitrogen atmosphere for 2 hours. After the evolution of hydrogen gas ceased, the mixture was cooled to 10° C. To this mixture was added dropwise an anhydrous N,N-dimethylformamide (150 ml) solution of 4-bromomethyl-2-chlorophenyl 2,2-dimethylpropanoate (10 g) at room temperature under stirring over 1 hour, and the mixture was stirred at 80° C. for 1 hour. After cooling, the reaction mixture was poured into ice water, which was extracted with ethyl acetate. The organic layer was washed with saturated aqueous ammonium chloride solution and then saturated sodium chloride solution, dried with anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography, which afforded 2-chloro-4-(2-2H-1,2,3-triazolyl)-methylphenyl 2,2-dimethylpropanoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05684022
Source datasetuspto-grants-1997_11
ORD IDord-964015d45a8b46b1ab4ef83c728c1796
Source noteuspto-grants-1997_11