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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2073327Generated: October 31, 2026

Benzaldehyde → 5,5-Bis(bromomethyl)-2-phenyl-1,3-dioxane

https://huagongshe.com/reaction/2073327

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantSulfuric AcidHCID 1118—
Reactant2,2-Bis(bromomethyl)-1,3-propanediolHCID 18692—
SolventBenzeneHCID 241—
Product5,5-Bis(bromomethyl)-2-phenyl-1,3-dioxaneHCID 2182307088.6%

Reaction Steps

2,2-Bis(bromomethyl)propane-1,3-diol (250 g) and benzaldehyde (110 g) were added to benzene (500 cm3) containing concentrated sulphuric acid (2 cm3) and the mixture boiled. Water was removed using a Dean Stark apparatus. After about 6 hours the reaction was complete. The mixture was cooled and the sulphuric acid neutralised by the addition of excess sodium bicarbonate. The resulting solution was filtered and the benzene removed under reduced pressure to give an oil which solidified on standing. Recrystallisation from petroleum ether gave the 1,3-dioxane (296 g) as a white solid (m.p. 66° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04916214
Source datasetuspto-grants-1990_04
ORD IDord-4550d0a6d92b4106909d601e2b4b7037
Source noteuspto-grants-1990_04