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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 269953Generated: October 25, 2026

Dimethyl Sulfoxide → 2-[1-(3-chloropropyl)-1H-indol-4-yloxy]-2-methylpropionic acid ethyl ester

https://huagongshe.com/reaction/269953

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
Reactant1-Bromo-3-chloropropaneHCID 8006—
ReactantPotassium HydroxideHCID 14797—
Reactant2-(1H-indol-4-yloxy)-2-methylpropionic acid ethyl esterHCID 16090870—
SolventWaterHCID 962—
Product2-[1-(3-chloropropyl)-1H-indol-4-yloxy]-2-methylpropionic acid ethyl esterHCID 1609087398%

Reaction Steps

2-(1H-Indol-4-yloxy)-2-methylpropionic acid ethyl ester (0.100 g, 0.40 mmol, 1.0 eq), powdered potassium hydroxide (0.034 g, 0.61 mmol, 1.5 eq), and DMSO (3 mL) were mixed and stirred at room temperature for 10 minutes. 1-Bromo-3-chloropropane (0.12 mL, 0.191 g, 1.21 mmol, 3.0 eq) was then added to the above mixture. The reaction mixture was stirred at room temperature for another 1.5 hours before 15 mL of water was added. The mixture was extracted with ethyl acetate (2×30 mL). The organic layer was collected, combined, washed with water (6×25 mL) and brine (2×20 mL), and dried over anhydrous Na2SO4. The solvent was removed in vacuo to afford 2-[1-(3-chloropropyl)-1H-indol-4-yloxy]-2-methylpropionic acid ethyl ester (0.127 g, yield: 97%) as a dense oily liquid, which was used for the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07449478B2
Source datasetuspto-grants-2008_11
ORD IDord-ac71b308e6764506acda086ceb619d3e
Source noteuspto-grants-2008_11