Identification | Back 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 Properties | Back 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 |
Hazard Information | Back Directory | [Synthesis]
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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SPIRO PHARMA
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www.spiropharma.com.cn |
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