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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1519737Generated: November 4, 2026

Tetrahydrofuran → HCID 86679295, compound

https://huagongshe.com/reaction/1519737

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium ChlorideHCID 25517—
ReactantTBAF tetrahydrofuranHCID 11078149—
ReactantHCID 86679294HCID 86679294—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductHCID 86679295HCID 8667929580.4%

Reaction Steps

A 1 mol/L-TBAF-THF solution (3.4 mL) was added dropwise, under ice cooling, to a mixture of 4-[(triisopropylsilanyl)ethynyl]furan-2-carbaldehyde (0.63 g) as obtained in Example 24-(1), THF (3.0 mL) and acetic acid (0.20 mL) over the course of 1.5 hours. Diethyl ether and water were added to the reaction mixture, and the mixture was adjusted to pH 5 with a saturated aqueous solution of ammonium chloride to isolate the organic layer. The extract was washed with brine, and the solvent was distilled off under reduced pressure. The resulting residue was purified by OH type silica gel column chromatography (gradient elution with hexane/ethyl acetate=100/0→80/20) to obtain 4-ethynylfuran-2-carbaldehyde (brown solid) (0.22 g, 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073821B2
Source datasetuspto-grants-2015_07
ORD IDord-8da6824a460d471bb5f12cff73285735
Source noteuspto-grants-2015_07