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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 247357Generated: October 25, 2026

Toluene → 2-Tert.-butyl-4,4,7,7,-tetramethyl-1,3-dioxacycloheptane

https://huagongshe.com/reaction/247357

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant2,5-Dimethyl-2,5-hexanediolHCID 8031—
ReactantPivalaldehydeHCID 12417—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventWaterHCID 962—
Product2-Tert.-butyl-4,4,7,7,-tetramethyl-1,3-dioxacycloheptaneHCID 1398074885%

Reaction Steps

A mixture of 730 g (5 mol) of 2,5-dimethylhexane-2,5-diol, 3 g of p-toluenesulfonic acid, 430 g (5 mol) of pivalaldehyde and 1 l of toluene was refluxed for 4 hours (h) during which the water of reaction produced (90 ml) was removed. The reaction mixture was then cooled down to room temperature (RT) and stirred up with 10 ml of 25% strength aqueous sodium hydroxide solution, the phases were separated, the organic phase was washed with a little water until neutral, and the toluene was then removed at 50°-60° C. The residue obtained was fractionated under reduced pressure affording 909 g (4.25 mol) of 2-tert.-butyl-4,4,7,7,-tetramethyl-1,3-dioxacycloheptane (boiling point 54° C./0.2 mbar). This corresponds to a yield of 85% of theory.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04707302
Source datasetuspto-grants-1987_11
ORD IDord-03ed008d92b34129a4600f2fd633702e
Source noteuspto-grants-1987_11