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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1268472Generated: November 1, 2026

Ethylene Glycol → 6-(2-methyl-1,3-dioxolan-2-yl)3,4-dihydro-4,4-dimethylnaphthalen-1(2H)-one

https://huagongshe.com/reaction/1268472

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant3,4-dihydro-4,4-dimethyl-6-acetyl-1(2H)-naphthalenoneHCID 11106782—
Reactant3,4-dihydro-4,4-dimethyl-7-acetyl-1(2H)-naphthalenoneHCID 22323726—
SolventBenzeneHCID 241—
Product6-(2-methyl-1,3-dioxolan-2-yl)3,4-dihydro-4,4-dimethylnaphthalen-1(2H)-oneHCID 15462843—

Reaction Steps

A solution of 1.80 g (8.34 mmol) of a 1:5 mixture of 3,4-dihydro-4,4-dimethyl-7-acetyl-naphthalen-1(2H)-one (Compound D14a); and 3,4-dihydro-4,4-dimethyl-6-acetyl-naphthalen-1(2H)-one (Compound D14b) in 50 mL benzene was combined with 517.7 mg (8.34 mmol) of ethylene glycol and 20.0 mg (0.11 mmol) of p-toluenesulfonic acid monohydrate. The resulting solution was heated to reflux for 18 h, cooled to room temperature, and concentrated under reduced pressure. The title compound was isolated by column chromatography (10% EtOAc-hexanes) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06555690B2
Source datasetuspto-grants-2003_04
ORD IDord-3e3bf27ad1d44dbe9c1d9c88a19e73c6
Source noteuspto-grants-2003_04