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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380638Generated: November 3, 2026

Hydrogen Bromide → 4H-1,3-Dioxin-4-one, 5-bromo-2,2,6-trimethyl-

https://huagongshe.com/reaction/1380638

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantBromineHCID 24408—
Reactant2,2,6-Trimethyl-4H-1,3-dioxin-4-oneHCID 79368—
ReactantDiethylether hexaneHCID 21584099—
SolventDichloromethaneHCID 6344—
Product4H-1,3-Dioxin-4-one, 5-bromo-2,2,6-trimethyl-HCID 1035343575%

Reaction Steps

Bromine (0.105 mol, 5.38 ml) was added dropwise to a 20° C. solution of 2,2,6-trimethyl-4H-1,3-dioxin-4-one (TKD, 0.1 mol, 14.2 g) in 100 ml CH2Cl2 over five minutes. The reaction solution was rapidly decolorized and hydrogen bromide evolved. After 15 minutes, the solvent was removed in vacuo to provide 22 g (99%, >95% pure by NMR) of a pale yellow oil which solidified upon refrigeration. Flash chromatography (10% ether/hexane on silica) afforded 16.5 g (75%) of the title compound as colorless plates.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04582913
Source datasetuspto-grants-1986_04
ORD IDord-c39d5e366b2f440fac5b146d43dae0f8
Source noteuspto-grants-1986_04