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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1289316Generated: November 2, 2026

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

https://huagongshe.com/reaction/1289316

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 numberUS05747542
Source datasetuspto-grants-1998_05
ORD IDord-686df1280a0448fe99919b81e114f461
Source noteuspto-grants-1998_05