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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl cyanoacetate | HCID 7764 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 5-Bromo-1-benzothiophene | HCID 2776578 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Catalyst | Triphenylphosphine | HCID 11776 | — |
| Catalyst | Sodium borohydride | HCID 4311764 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Benzo[b]thiophene-5-acetic acid | HCID 11469582 | 74.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08273902B2 |
|---|
| Source dataset | uspto-grants-2012_09 |
|---|
| ORD ID | ord-61efb90e244e46f69ca76915f0db613a |
|---|
| Source note | uspto-grants-2012_09 |
|---|