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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1863831Erstellt: 26. Oktober 2026

(1,4-Phenylenebis(methylene))bis(triphenylphosphonium) dibromide → 1,1'-[1,4-Phenylenedi(ethene-2,1-diyl)]bis[4-(pentadecyloxy)benzene]

https://huagongshe.com/reaction/1863831

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(1,4-Phenylenebis(methylene))bis(triphenylphosphonium) dibromideHCID 2723797—
Eduktp-PentadecanoxybenzaldehydeHCID 23127399—
LösungsmittelMethanolHCID 887—
Produkt1,1'-[1,4-Phenylenedi(ethene-2,1-diyl)]bis[4-(pentadecyloxy)benzene]HCID 5797294692,9%

Reaktionsschritte

A 30-ml four-necked flask was used, 7.87 g (23.7 mM) of p-pentadecanoxybenzaldehyde synthesized as described above and 8.65 g (11.0 mM) of p-xylylenebis(triphenylphosphonium bromide) were suspended in 100 ml of methanol, and 6.87 g (35.6 mM) of 28-percent by weight methylate was dropped thereto at room temperature (25° C.). Thereafter, aging was performed at a reflux temperature of 65° C. for 3 hours. Methanol was distilled out, and 200 ml of water was added to the residue, followed by agitation. Subsequently, the precipitate was filtrated. The resulting precipitate was further washed with water and acetone, followed by drying, so as to produce 7.49 g of 1,4-bis(4′-pentadecanoxystyryl)benzene isomer mixture (Compound (7)).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07625499B2
Quelldatensatzuspto-grants-2009_12
ORD IDord-28e86a10ab5f40e7a68ea9e22227d7fa
Quellennotizuspto-grants-2009_12