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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2390964Generated: October 29, 2026

Ethyl cyanoacetate → Benzo[b]thiophene-5-acetic acid

https://huagongshe.com/reaction/2390964

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl cyanoacetateHCID 7764—
ReactantSodium HydroxideHCID 14798—
Reactant5-Bromo-1-benzothiopheneHCID 2776578—
ReactantPotassium tert-butoxideHCID 23665647—
CatalystTriphenylphosphineHCID 11776—
CatalystSodium borohydrideHCID 4311764—
CatalystHCID 178418397HCID 178418397—
CatalystHCID 178418476HCID 178418476—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductBenzo[b]thiophene-5-acetic acidHCID 1146958274.9%

Reaction Steps

To toluene (25 mL) suspension of 0.16 g of dichlorobis(triphenylphosphine)palladium(II) were added 0.12 g of triphenylphosphine, 0.01 g of sodium borohydride, 5.79 g of potassium tert-butoxide and 2.92 g of ethyl cyanoacetate, which was then stirred at room temperature for 10 minutes. Thereto were added 5.00 g of 5-bromobenzothiophene and 25 mL of toluene, which was then refluxed for 4 hours. Thereto was added 0.14 g of tetrakis(triphenylphosphine)palladium(0), which was then refluxed for 2 hours. Next, to the reaction solution were added 25 mL of ethanol, 2.82 g of sodium hydroxide and 5 mL of water, which was then refluxed for 6 hours. Thereto was added 2.82 g of sodium hydroxide, which was then refluxed for 5 hours. To the reaction mixture were added 15 mL of water and 0.5 g of activated carbon, and insoluble matter was filtered off. The aqueous layer was separated, and to the solution was added 35 mL of ethanol. The pH was adjusted to 2 with 15 mL of hydrochloric acid. Thereto was added 15 mL of water, which was then stirred at 40° C. Thereto was added 30 mL of water, which was stirred. After that, it was cooled. The precipitate was collected by filtration to provide 3.38 g of 2-(1-benzothiophen-5-yl)acetic acid as pale yellow solid form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273902B2
Source datasetuspto-grants-2012_09
ORD IDord-61efb90e244e46f69ca76915f0db613a
Source noteuspto-grants-2012_09