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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1901548Generated: October 31, 2026

1,2-Dimethoxyethane → HCID 23368329, compound

https://huagongshe.com/reaction/1901548

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantPotassium bisulfideHCID 102109—
Reactant1-Propyne, 3-(chloromethoxy)-HCID 12241341—
ReactantHCID 23368334HCID 23368334—
SolventWaterHCID 962—
ProductHCID 23368329HCID 23368329—

Reaction Steps

2.18 Grams of 3-methyl-4-cyano-5-methylsulfonylisothiazole was dissolved in 20 ml of dimethoxyethane, and a solution of 1.2 g of potassium hydrosulfide (KSH) in 5 ml of water was added at room temperature with stirring. After stirring for 10 minutes, 1.3 g of 2-propynyloxymethyl chloride was added, and the reaction solution was stirred for 3 hours. Water was added to the reaction solution, which was then extracted with ethyl acetate. The extract was washed with water, dried and concentrated to obtain 2.1 g of an oily 3-methoxy-4-cyano-5-(2-propynyloxymethylthio)isothiazole. This product was dissolved in 20 ml of DMF and ice-cooled to 5° to 10° C. To this solution was added a solution of 5.1 g of iodine and 3.2 g of potassium iodide in 5 ml of water and 10 ml of DMF, and then 6.6 g of a 10% KOH was added dropwise. After addition, the reaction solution was stirred for 2 hours until the temperature reached room temperature. Water was added to the reaction solution, which was then extracted with ethyl acetate. The extract was washed with water, dried and concentrated under reduced pressure to obtain an oily product. This product was recrystallized from ether to obtain 2.7 g of white crystals having a melting point of 124° to 125° C. (yield 76%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05578622
Source datasetuspto-grants-1996_11
ORD IDord-5ab8d0a591e34ba287dbb51bc93a52ce
Source noteuspto-grants-1996_11