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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 890553Erstellt: 23. Oktober 2026

Potassium Hydroxide → 4-Ethynylbenzoic acid

https://huagongshe.com/de/reaction/890553

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium HydroxideHCID 14797—
Edukt4-[(Trimethylsilyl)ethynyl]benzoic acidHCID 13628190—
LösungsmittelMethanolHCID 887—
Produkt4-Ethynylbenzoic acidHCID 58970696%

Reaktionsschritte

Initially, 4-bromoacetophenone (3) can be treated with powdered phosphorous pentachloride to produce 1-(4-bromophenyl)-1-chloroethylene (4). Compound 4 was then treated with potassium hydroxide to produce 4-bromophenylacetylene (5) at a 60% yield. Treatment of compound 5 with ethyl magnesium bromide was followed by reaction with chlorotrimethylsilane. The resulting product (4-bromophenylethynyl) trimethylsilane (6) was recovered with a 90% yield. Compound 6 was then treated with ethyl magnesium bromide, followed by reaction with carbon dioxide to produce (4-carboxyphenylethynyl) trimethylsilane (7) in 89% yield. Compound 7 was then deprotected using KOH in methanol to form 4-ethynylbenzoic acid (8) in 96% yield. Compound 8 is a useful building block for forming a variety of molecular switches in accordance with the present invention, and was used in forming molecular switches of the following examples.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06995312B2
Quelldatensatzuspto-grants-2006_02
ORD IDord-a0da8d7a8c144929a6db5478c0fa0491
Quellennotizuspto-grants-2006_02