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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424779Generated: October 29, 2026

Diethyl Ether → 3-(2,6-Dichloro-phenyl)-3H-[1,2,3]triazole-4-carbaldehyde

https://huagongshe.com/reaction/424779

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantSodium HydroxideHCID 14798—
ReactantTriacetoxyperiodinaneHCID 159087—
ReactantHCID 66704184HCID 66704184—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product3-(2,6-Dichloro-phenyl)-3H-[1,2,3]triazole-4-carbaldehydeHCID 8662925094.9%

Reaction Steps

To a solution of [3-(2,6-dichloro-phenyl)-3H-[1,2,3]triazol-4-yl]-methanol (1.87 g, 1 equiv) in methylene chloride (110 mL) is added Dess-Martin oxidant (4.20 g, 1.3 equiv). The reaction mixture is allowed to stir at room temperature for 3 h. The reaction is incomplete as evidenced by TLC. The reaction mixture is treated with Dess-Martin oxidant (1.20 g). The reaction mixture is allowed to stir at room temperature for an additional 2 h. The reaction mixture is treated with 80 mL 1.5 N sodium hydroxide and 40 mL diethyl ether. The resulting solution is allowed to stir at room temperature for ten minutes. The reaction mixture is diluted with 120 mL water and extracted three times with chloroform. The combined organic layers are dried over magnesium sulfate and filtered though a plug of silica gel eluting with chloroform/ethyl acetate (3:1, 200 mL). The filtrate is concentrated under reduced pressure to give the title compound (1.76 g, 94%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106077B2
Source datasetuspto-grants-2012_01
ORD IDord-f4fdec5c5f3b49c58e0085fc5293ced5
Source noteuspto-grants-2012_01