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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1651652Generated: October 26, 2026

1-(Chloromethoxy)-2-methoxyethane → 2-[1-(Methoxyethoxymethoxy)ethyl]-3-methylthiothiophene

https://huagongshe.com/reaction/1651652

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Chloromethoxy)-2-methoxyethaneHCID 77590—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-(1-Hydroxyethyl)3-methylthiothiopheneHCID 23050277—
SolventDichloromethaneHCID 6344—
Product2-[1-(Methoxyethoxymethoxy)ethyl]-3-methylthiothiopheneHCID 5410565287.1%

Reaction Steps

To a stirred solution of 2-(1-hydroxyethyl)3-methylthiothiophene (13.5 g, 0.077 mol) in dry methylene chloride (100 ml) was added methoxyethoxymethyl chloride (11.5 g, 0.092 mol) followed by N,N-diisopropylethylamine (12.1 g, 0.092 mol) with cooling. The solution was stirred at room temperature for 18 hours. Some starting material remained upon work up at this point. The material was recycled as above using 1/2 the above quantities of methoxyethoxymethyl chloride and N,N-diisopropylethyl amine. After 5 hours at room temperature the reaction was completed. The solution was washed with water, dilute HCl, saturated NaHCO3 solution and again with water. Then it was dried over anhydrous Na2SO4, filtered and concentrated in vacuo. Pure product was obtained as a yellow oil (17.6 g, 87%). TLC confirmed the purity and NMR and mass spectrometry (M/Z=262) supported the structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04929637
Source datasetuspto-grants-1990_05
ORD IDord-f59b579c31c041e8baf034b25603ad51
Source noteuspto-grants-1990_05