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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507742Generated: November 4, 2026

Neopentyl glycol → 2-(4-Bromophenyl)-5,5-dimethyl-1,3-dioxane

https://huagongshe.com/reaction/507742

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNeopentyl glycolHCID 31344—
Reactant4-BromobenzaldehydeHCID 70741—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventBenzeneHCID 241—
Product2-(4-Bromophenyl)-5,5-dimethyl-1,3-dioxaneHCID 1371451593%

Reaction Steps

A mixture of 4-bromobenzaldehyde (100 g, 0.54 mole), neopentyl glycol (115 g, 1.10 mole), and p-toluenesulfonic acid (800 mg, 4 mmole) in benzene (800 mL) was heated to reflux using a Dean Stark apparatus for 16 h. The reaction mixture was cooled to room temperature and most of the benzene was removed. The residue was partitioned between ethyl acetate (500 mL) and cold water (150 mL). The organic phase was washed with water (2×150 mL) and brine (1×150 mL), then dried (Na2SO4) and concentrated to give the desired product (136 g, 93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786112B2
Source datasetuspto-grants-2010_08
ORD IDord-1146809866274295b6e3a0bb7a28a812
Source noteuspto-grants-2010_08