HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 408560Generated: October 30, 2026
Hydrochloric Acid → HCID 66751041, compound
https://huagongshe.com/reaction/408560
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | tert-Butyl cyanoacetate | HCID 70693 | — |
| Reactant | 4-Bromobenzo[b]thiophene | HCID 12094208 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 66751041 | HCID 66751041 | — |
Reaction Steps
To a solution of 4-bromobenzothiophene (1 eq.) in DME were added tert-butyl cyanoacetate (1.1 eq.) and t-BuOK (2 eq.). The reaction was refluxed for 40 min. Thereto were added dichlorobis(triphenylphosphine)palladium(II) (0.02 eq.) and triphenylphosphine (0.06 eq.). The resulting mixture was refluxed for 1.5 h under argon and then cooled to 20° C. Aqueous HCl (6N) was added dropwise until pH=1 and the reaction mixture was partitioned between water and EtOAc. The organic layer was separated, dried over MgSO4, filtered and concentrated under reduced pressure. The crude was purified by chromatography on silica gel (elution with heptane/DCM: 9/1 to 1/1) to afford benzo[b]thiophen-4-yl-cyano-acetic acid tert-butyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08759334B2 |
|---|
| Source dataset | uspto-grants-2014_06 |
|---|
| ORD ID | ord-719985b2e402402b83bf0808ae4543fd |
|---|
| Source note | uspto-grants-2014_06 |
|---|