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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242394Generated: October 26, 2026

Ethylene Glycol → HCID 58418115, compound

https://huagongshe.com/reaction/242394

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant5-Bromo-4-methylthiophene-2-carbaldehydeHCID 16414192—
SolventTolueneHCID 1140—
ProductHCID 58418115HCID 58418115—

Reaction Steps

Ethylene glycol (2.18 ml) and p-toluenesulfonic acid (0.74 g) is added to a solution of 2-brom-3-methyl-5-formylthiophene (4.0 g) in toluene (98 ml) in a Dean-Stark apparatus. After 18 hours at reflux, the reaction is quenched with water. The organic phase is separated and the aqueous phase is extracted three times with ethyl acetate. The combined organic phases are dried over Na2SO4 and concentrated in vacuo. The crude product is purified on a semi-preparative HPLC to yield 2-(5-bromo-4-methyl-thiophen-2-yl)-[1,3]dioxolane (4.04 g) as a yellow oil. MS (HPLC/MS): 250 (MH+). Retention time: 4.02 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653116B2
Source datasetuspto-grants-2014_02
ORD IDord-a2f33a69762c4e04b35517459d35e114
Source noteuspto-grants-2014_02