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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 851621Generated: October 27, 2026

2-Bromo-1-(5-methyl-1,3-dioxan-5-yl)ethan-1-one → 1-(5-Methyl-1,3-dioxan-5-yl)-2-(1,2,4-triazol-1-yl)-ethan-1-one

https://huagongshe.com/reaction/851621

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-1-(5-methyl-1,3-dioxan-5-yl)ethan-1-oneHCID 12855651—
Reactant1,2,4-TriazolylsodiumHCID 54719965—
SolventTetrahydrofuranHCID 8028—
Product1-(5-Methyl-1,3-dioxan-5-yl)-2-(1,2,4-triazol-1-yl)-ethan-1-oneHCID 1285565287.2%

Reaction Steps

A solution of 223 g (1 mole) of 1-(5-methyl-1,3-dioxan-5-yl)-2-bromoethan-1-one in 200 ml of tetrahydrofuran is added dropwise in the course of 2 hours, at 25° C., to a suspension, which is stirred under pure nitrogen, of 100.1 g (1.1 moles) of sodium 1,2,4-triazolide in 300 ml of dry tetrahydrofuran. After refluxing the mixture for eight hours, the inorganic precipitate is filtered off and the filtrate is concentrated to half its volume. The mixture is seeded and left to stand overnight at +3° C. The precipitate is filtered off, washed with 30 ml of cold tetrahydrofuran (at +5° C.), then with 80 ml of ether and thereafter with 100 ml of n-pentane, and dried. 184 g (87.2%) of 1-(5-methyl-1,3-dioxan-5-yl)-2-(1,2,4-triazol-1-yl)-ethan-1-one are obtained as white crystals of melting point 95°-97° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04385925
Source datasetuspto-grants-1983_05
ORD IDord-c60dd0aadbc64e319974943f21535ec0
Source noteuspto-grants-1983_05