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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 847001Generated: October 26, 2026

Carbon tetrabromide → 5-Bromomethyl-2-phenyl-1,3-dioxane

https://huagongshe.com/reaction/847001

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
Reactant(2-Phenyl-1,3-dioxan-5-yl)methanolHCID 10679342—
SolventBenzeneHCID 241—
Product5-Bromomethyl-2-phenyl-1,3-dioxaneHCID 1483510175.6%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a vigorously stirred solution of 19.4 g (0.1M) of 5-hydroxymethyl-2-phenyl-1,3-dioxane ml and 33.1 g (0.1M) of tetrabromomethane in 60 ml of anhydrous benzene at 70° C., is added 26.2 g (0.1M) of triphenylphosphine in 45 minutes. After stirring at 70° C. for an another 30 minutes, the solvent is evaporated. To the residue is added 200 ml of ether and ether insoluble triphenylphosphine oxide is removed by filtration. After repeating this procedure twice, the solvent of the filtrated is evaporated. Distillation of the residual product gives 19.391 g (75.4% yield) of the titled compound m2. B.P. 145°~158° C. (1 mmHg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05138067
Source datasetuspto-grants-1992_08
ORD IDord-6ed750b70a2c44d0ac4df7c84ece783f
Source noteuspto-grants-1992_08