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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 408560Generated: October 30, 2026

Hydrochloric Acid → HCID 66751041, compound

https://huagongshe.com/reaction/408560

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriphenylphosphineHCID 11776—
Reactanttert-Butyl cyanoacetateHCID 70693—
Reactant4-Bromobenzo[b]thiopheneHCID 12094208—
ReactantPotassium tert-butoxideHCID 23665647—
CatalystHCID 178418476HCID 178418476—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 66751041HCID 66751041—

Reaction Conditions

Temperature20 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759334B2
Source datasetuspto-grants-2014_06
ORD IDord-719985b2e402402b83bf0808ae4543fd
Source noteuspto-grants-2014_06