Welcome to chemicalbook!
Chinese English Japanese Germany Korea
400-158-6606
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

10-broMoanthracene-9-carboxylic acid synthesis

4synthesis methods
-

Yield: 90%

Reaction Conditions:

with bromine;acetic acid at 60; for 4 h;

Steps:

1
9-anthracenecarboxylic acid (7.40 g, 3.33 mmol), acetic acid (AcOH, 0.6 L), bromine (Br 2, 1.8 ml) were placed in a reaction vessel and stirred at 60 ° C. for 4 hours for reaction .After completion of the reaction, the reaction product was added to 1.0 L of water saturated with potassium carbonate (K 2 CO 3) and stirred. The resulting solution was neutralized with concentrated hydrochloric acid with sufficient stirring to give a bright yellow precipitate. While thoroughly washing the precipitate with water, it was collected by filtration and dried under reduced pressure to obtain yellow powder 1 (10-bromoanthracene-9-carboxylic acid, 9.0 g) (yield: 90%).

References:

TOYOTA CENTRAL R&D LABS INCORPORATED;MOTEGI, HIROFUMI;SHICHI, AKIRA;MUKAE, YUSUKE;IDOTA, YOSHINORI JP2016/222632, 2016, A Location in patent:Paragraph 0035-0037