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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 37760Erstellt: 24. Oktober 2026

Bromine → 2,7-Bis-(but-2-enoyl)-thioxanthen-9-one

https://huagongshe.com/de/reaction/37760

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBromineHCID 24408—
EduktThioxantheneHCID 67495—
Edukttrans-Crotonyl chlorideHCID 643131—
EduktAluminum(III) ChlorideHCID 6451240—
Edukt1-[7-(but-2-enoyl)-9H-thioxanthen-2-yl]-but-2-en-1-oneHCID 68597883—
KatalysatorTetrabutylammonium BromideHCID 74236—
LösungsmittelDichloromethaneHCID 6344—
Produkt2,7-Bis-(but-2-enoyl)-thioxanthen-9-oneHCID 68596945—

Reaktionsschritte

To 1-[7-(but-2-enoyl)-9H-thioxanthen-2-yl]-but-2-en-1-one, which is synthesized by thioxanthene and crotonoyl chloride in the presence of aluminium chloride as described in WO2005-080337A1, dissolved in dichloromethane are added bromine (2.0 equiv.) and aqueous tetra-n-butylammonium bromide (0.5 equiv.). Stirring the reaction mixture at room temperature and succeeding extractive work-up and purification give 2,7-bis-(but-2-enoyl)-thioxanthen-9-one, which is transformed into the compound of example 9 as described in example 4.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08524425B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-1484c856a3ab479daf9d33fbc09ffbee
Quellennotizuspto-grants-2013_09