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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1979822Generated: October 31, 2026

Ethylene Glycol → HCID 12813211, compound

https://huagongshe.com/reaction/1979822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantHCID 13151117HCID 13151117—
SolventBenzeneHCID 241—
ProductHCID 12813211HCID 12813211—

Reaction Steps

Treatment of 1-benzyloxy-4-(1,3-dithian-2-yl)-butan-2-one (89.8 g) in benzene (3.5 l) with distilled ethylene glycol (220 ml) and p-toluenesulfonic acid (11.7 g) at reflux temperature in a Dean-Stark apparatus for 18 hours gives a mixture which is concentrated to 500 ml in vacuo and allowed to stir for one hour. After the addition of sodium carbonate (10 g), the mixture is then partitioned between ether (300 ml) and brine (300 ml). The aqueous phase is extracted with ether (600 ml) and the combined extracts are washed with 0.05% sodium carbonate (1.2 l), filtered through phase-separating paper and dried (sodium sulfate). The solvent is removed in vacuo to give a residue (102.15 g; 99%). A 200 mg portion of the residue is purified on Quantagram PQ1F plates (chloroform) to give 1-benzyloxy-2,2-ethylenedioxy-4-(1,3-dithian-2-yl)-butane (180 mg);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04482730
Source datasetuspto-grants-1984_11
ORD IDord-6a9c98f8854540dfabafc3f7a8e96649
Source noteuspto-grants-1984_11