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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 85301Erstellt: 24. Oktober 2026

Chloroform → 2-[2-(2,4,6-Trimethoxyphenyl)vinyl]thiophene

https://huagongshe.com/de/reaction/85301

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChloroformHCID 6212—
Edukt2,4,6-TrimethoxybenzaldehydeHCID 70019—
EduktTriphenyl(2-thienylmethyl)phosphonium BromideHCID 10741697—
EduktHCID 178506676HCID 178506676—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-[2-(2,4,6-Trimethoxyphenyl)vinyl]thiopheneHCID 6800864992,8%

Reaktionsschritte

In a stream of argon, to 30 ml of tetrahydrofuran was added 0.95 g of phenyllithium (19% solution in dibutylether) (2.15 mmol). To this mixture, 0.78 g (1.98 mmol) of thiophene-2-ylmethyltriphenylphosphonium bromide was added under cooling. After the mixture was well-stirred, 0.38 g (1.98 mmol) of 2,4,6-trimethoxybenzaldehyde dissolved in 3 ml of tetrahydrofuran was added dropwise. The mixture was reacted with stirring for 1.5 hours. After the reaction mixture was poured into 70 ml of ice water, extraction with 200 ml of chloroform, washing with a saturated saline solution, drying over anhydrous magnesium sulfate, and concentration were performed. The residue was purified by silica gel chromatography to give 508 mg (yield: 92%) of 2-[2-(2,4,6-trimethoxyphenyl)vinyl]thiophene as a colorless crystal.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08846955B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-aaf7754e66d54ee3b720359ff69a7970
Quellennotizuspto-grants-2014_09