1H-Indole-3-aceticacid,4-bromo-(9CI)
1H-Indole-3-aceticacid,4-bromo-(9CI) Basic information
- Product Name:
- 1H-Indole-3-aceticacid,4-bromo-(9CI)
- Synonyms:
-
- 1H-Indole-3-aceticacid,4-bromo-(9CI)
- 4-broMo-1H-indole-3-acetic acid
- 4-Bromo-3-indoleacetic acid
- 2-(4-bromo-1H-indol-3-yl)acetic acid
- 1H-Indole-3-acetic acid, 4-broMo-
- (4-Bromo-1H-indol-3-yl)-acetic acid
- 4-Bromoindole-3-acetic Acid
- CAS:
- 89245-41-0
- MF:
- C10H8BrNO2
- MW:
- 254.08
- Product Categories:
-
- INDOLE
- Mol File:
- 89245-41-0.mol
1H-Indole-3-aceticacid,4-bromo-(9CI) Chemical Properties
- 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
1H-Indole-3-aceticacid,4-bromo-(9CI) Usage And Synthesis
Synthesis
65018-18-0
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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1H-Indole-3-aceticacid,4-bromo-(9CI)(89245-41-0)Related Product Information
- 4-BROMO-1-(TERT-BUTOXYCARBONYL)-1H-INDOLE-3-CARBOXYLIC ACID
- methyl 4-bromo-1H-indole-3-carboxylate
- 1H-Indazole-3-carboxaldehyde, 4-broMo-
- 4-Bromoindole-3-carboxaldehyde
- 4-Bromo-2-indolecarboxylic acid
- 4-BROMOOXINDOLE
- 4-BROMOINDOLE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
- 4-Bromoindole-2-carboxylic acid methyl ester
- 4-BROMOTRYPTOPHOL
- (4-BROMO-1H-INDOL-3-YL)-ACETIC ACID METHYL ESTER
- 1H-Indole-3-aceticacid,4-bromo-(9CI)