Basic information Safety Supplier Related

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

Basic information Safety Supplier Related

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
More
Less

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
More
Less

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

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

Accela ChemBio Co.,Ltd.
Tel
021-50795510 4000665055
Email
sales@accelachem.com
Shandong Xiya Chemical Co., Ltd
Tel
4009903999 13355009207
Email
3007715519@qq.com
Hangzhou Sage Chemical Co., Ltd.
Tel
+86057186818502 13588463833
Email
info@sagechem.com
Shanghai Topbiochem Technology Co., Ltd
Tel
021-58170097
Email
info@topbiochem.com
9ding chemical ( Shanghai) Limited
Tel
4009209199
Email
sales@9dingchem.com