Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2166996Generated: November 2, 2026

Ethylene Glycol → 2-(5-Bromo-4-methylthiophen-2-yl)-1,3-dioxolane

https://huagongshe.com/reaction/2166996

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant5-Bromo-4-methylthiophene-2-carbaldehydeHCID 16414192—
SolventTolueneHCID 1140—
Product2-(5-Bromo-4-methylthiophen-2-yl)-1,3-dioxolaneHCID 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 numberUS09044389B2
Source datasetuspto-grants-2015_06
ORD IDord-86f0397b59dd43bcb494eed53798f889
Source noteuspto-grants-2015_06