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ChemicalBook--->CAS DataBase List--->89245-41-0

89245-41-0

89245-41-0 Structure

89245-41-0 Structure
IdentificationBack Directory
[Name]

1H-Indole-3-aceticacid,4-bromo-(9CI)
[CAS]

89245-41-0
[Synonyms]

4-Bromo-3-indoleacetic acid
4-Bromoindole-3-acetic Acid
4-broMo-1H-indole-3-acetic acid
1H-Indole-3-acetic acid, 4-broMo-
(4-Bromo-1H-indol-3-yl)-acetic acid
1H-Indole-3-aceticacid,4-bromo-(9CI)
2-(4-bromo-1H-indol-3-yl)acetic acid
[Molecular Formula]

C10H8BrNO2
[MDL Number]

MFCD09751717
[MOL File]

89245-41-0.mol
[Molecular Weight]

254.08
Chemical PropertiesBack Directory
[Melting point ]

185-187℃ (DEC.)
[Boiling point ]

466.0±30.0 °C(Predicted)
[density ]

1.746
[storage temp. ]

2-8°C
[pka]

4.27±0.30(Predicted)
[Appearance]

Light yellow to yellow Solid
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

1H-Indole-3-aceticacid,4-bromo-(9CI)(89245-41-0)1HNMR
Hazard InformationBack Directory
[Synthesis]

1H-Indole, 1,3-diacetyl-4-bromo-

65018-18-0

1H-Indole-3-aceticacid,4-bromo-(9CI)

89245-41-0

To a dry three-necked flask was added 98.0 kg of 4-bromoindole, 307.0 kg of aluminum trichloride and 500 L of methylene chloride, and 79.0 kg of acetyl chloride was added slowly and dropwise to the three-necked flask. The reaction mixture was heated to 40 °C and kept for 8 hours. Upon completion of the reaction, the mixture was poured into 800 L of ice water, the organic phase was separated and the solvent was recovered to give 1,3-diacetyl-4-bromoindole. Subsequently, 161 kg of morpholine and 40.0 kg of sulfur were added directly to the reaction system, heated to 120 °C and kept for 5 hours. After the rearrangement reaction was completed, 500 L of methanol was added, heated to dissolve, decolorized with activated carbon, filtered and cooled. To the filtrate, 300 L of 70% ethanol and 200 L of 15% sodium hydroxide solution were added and heated to reflux for 4 hours. After completion of the reaction, filter and recover the solvent under vacuum. To the residue, appropriate amount of water was added and the pH was adjusted to 1-2 with dilute hydrochloric acid to precipitate a solid. It was filtered, washed with water to neutral, and finally recrystallized with 60% ethanol to obtain 102.2 kg of 4-bromoindole-3-acetic acid in 85.2% yield.

[References]

[1] Patent: CN104311469, 2016, B. Location in patent: Paragraph 0070-0072
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