Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186366Generated: October 29, 2026

2-Benzofurancarboxaldehyde → HCID 65816420, compound

https://huagongshe.com/reaction/1186366

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BenzofurancarboxaldehydeHCID 61341—
Reactant(Trifluoromethyl)trimethylsilaneHCID 552549—
ReactantTetrabutylammonium FluorideHCID 2724141—
SolventTetrahydrofuranHCID 8028—
ProductHCID 65816420HCID 6581642044%

Reaction Steps

According to Reference Example 8-12, by use of benzofuran-2-carbaldehyde (300 mg, 2.05 mmol) dissolved in tetrahydrofuran (6 mL), a 1 mol/L solution of tetrabutylammonium fluoride in tetrahydrofuran (1.03 mL, 1.03 mmol) and (trifluoromethyl)trimethylsilane (0.516 mL, 3.49 mmol), the mixture was stirred and reacted at room temperature for 5 hours. Then, purification by preparative thin-layer chromatography (chloroform/methanol=100/1) was performed to give 1-(benzofuran-2-yl)-2,2,2-trifluoroethanol (Compound DR) (194 mg, yield: 44%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673908B2
Source datasetuspto-grants-2014_03
ORD IDord-22b7e932b1844c65bcb2bf7ed6e93a8c
Source noteuspto-grants-2014_03