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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 556136Erstellt: 25. Oktober 2026

Tetrahydrofuran → 1,4-Diethynylbenzene

https://huagongshe.com/reaction/556136

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrahydrofuranHCID 8028—
EduktTriethylamineHCID 8471—
Eduktp-DiiodobenzeneHCID 12208—
EduktTrimethylsilylacetyleneHCID 66111—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
KatalysatorHCID 178418476HCID 178418476—
LösungsmittelDichloromethaneHCID 6344—
Produkt1,4-DiethynylbenzeneHCID 120463—

Reaktionsschritte

Firstly, a mixture of 1,4-diiodobenzene (4 g, 12.1 mmol), PdCl2(PPh3)2 (340 mg, 0.484 mmol) and CuI (92.4 mg, 0.484 mmol), was added with dist. THF (20 mL), dist. Et3N (60 mL) and trimethylsilylacetylene (3.77 mL, 26.7 mmol). The resultant mixture was stirred under a nitrogen atmosphere at 80° C. for 22 hours to obtain a reaction mixture. Then, the reaction mixture was diluted with CH2Cl2. After that, an organic layer was washed with sat. NaCl, and dried with MgSO4. The dried organic layer was filtered and concentrated to obtain a crude product. The obtained crude product was separated and purified by silica gel column chromatography (hexane/EtOAc=10/1) to obtain 1,4-diethynylbenzene.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08053588B2
Quelldatensatzuspto-grants-2011_11
ORD IDord-6034d2caa9fe431b851a0cf58f3e4f58
Quellennotizuspto-grants-2011_11