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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 553217Generated: October 31, 2026

Hydrochloric Acid → Propyl 3-(2-(1-benzothiophen-5-yl)ethoxy)propionate

https://huagongshe.com/reaction/553217

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantSulfuric AcidHCID 1118—
ReactantAcrylonitrileHCID 7855—
ReactantBenzyltrimethylammonium hydroxideHCID 66854—
Reactant2-(1-Benzothiophen-5-yl)ethan-1-olHCID 11983371—
Solvent1-PropanolHCID 1031—
SolventTolueneHCID 1140—
ProductPropyl 3-(2-(1-benzothiophen-5-yl)ethoxy)propionateHCID 57615042—

Reaction Conditions

Temperature10 °C

Reaction Steps

To toluene (5 mL) suspension of 0.23 g of 40% (w/w) benzyltrimethylammonium hydroxide aqueous solution was added 5.00 g of 2-(1-benzothiophen-5-yl)ethanol, and dropwise added 2.20 mL of acrylonitrile at 0 to 5° C., which was then stirred at 0 to 20° C. for 1 hour. To this reaction mixture was added 0.125 mL of hydrochloric acid. Thereto were added 10 mL of propanol, 1.0 mL of water and 3.1 mL of sulfuric acid, which was then refluxed for 6.5 hours. After cooling, to the reaction mixture were added 10 mL of water and 10 mL of toluene. The organic layer was separated, and dried over anhydrous magnesium sulfate. After insoluble matter was filtered off, the solvent was distilled off under reduced pressure. The resultant residue was purified using silica gel column chromatography (eluent; hexane:ethyl acetate=15:1 to 7:1) to provide 7.21 g of propyl 3-(2-(1-benzothiophen-5-yl)ethoxy)propionate as colorless oily form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07951963B2
Source datasetuspto-grants-2011_05
ORD IDord-a679cd9622ec492c9aa51d7567227f4d
Source noteuspto-grants-2011_05