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ChemicalBook CAS DataBase List Rhodamine B
81-88-9

Rhodamine B synthesis

7synthesis methods
-

Yield:81-88-9 35 g

Reaction Conditions:

Stage #1: phthalic anhydride;3-diethylaminophenol in 1,2-dichloro-benzene at 175; for 13 h;
Stage #2: with water;sodium hydroxide at 25; for 0.5 h;
Stage #3: with hydrogenchloride;sodium chloride in water at 80; for 1 h;

Steps:

2.1 10063] Synthesis Example 2. Synthesis of compound of [Chemical Formula 4]

10063] Synthesis Example[Chemical Formula 4]10064] (1) Afier adding phthalic anhydride (15.7 g) and3-(N,N-dimethylamino)phenol (18.0 g) to 1 ,2-dichloroben- zene (57.0 g) in a reactor, the resulting mixture was stirred at 175° C. for 1 hout 1 hour later, 3-(N,N-diethylamino)phenol (12.1 g) was added in three aliquots. Afier the addition was completed, the mixture was stirred at 175° C. for 12 hours. Upon completion of reaction, the mixture was cooled to below 25°C. and, afier adding 3% sodium hydroxide aqueous solution (100 g), stirred for 30 minutes. After separating the organic layer and adding 4.5% sulfuric acid (330 g), the mixture was stirred for 30 minutes. Afier separating the aqueous layer and adding 35% hydrochloric acid (30 g) and sodium chloride (15 g), the mixture was stirred at 80° C. for 1 hour. After cooling to room temperature, the resulting crystals were filtered, washed with 2%: hydrochloric acid (300 g) and dried at 80° C. to obtain a compound of [Chemical Formula Di (35 g).

References:

US2015/322265,2015,A1 Location in patent:Paragraph 0064

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