Basic information Safety Supplier Related

5-Bromotryptophol

Basic information Safety Supplier Related

5-Bromotryptophol Basic information

Product Name:
5-Bromotryptophol
Synonyms:
  • 2-(5-BROMO-1H-INDOL-3-YL)-1-ETHANOL
  • 5-BROMOTRYPTOPHOL
  • 5-bromo-1H-indole-3-ethanol
  • 2-(5-Bromo-1H-indol-3-yl)ethanol
  • 5-Bromo-3-(2-hydroxyethyl)-1H-indole
  • L806 5-Bromotryptophol
  • 1H-Indole-3-ethanol, 5-bromo-
  • 5-Bromoindole-3-ethanol
CAS:
32774-29-1
MF:
C10H10BrNO
MW:
240.1
EINECS:
251-205-9
Mol File:
32774-29-1.mol
More
Less

5-Bromotryptophol Chemical Properties

Melting point:
92-94°C
Boiling point:
411.5±30.0 °C(Predicted)
Density 
1.618±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
form 
powder to crystal
pka
14.87±0.10(Predicted)
color 
White to Orange to Green
CAS DataBase Reference
32774-29-1(CAS DataBase Reference)
More
Less

Safety Information

Hazard Codes 
Xi
HazardClass 
IRRITANT
HS Code 
2933998090
More
Less

5-Bromotryptophol Usage And Synthesis

Synthesis

117235-22-0

32774-29-1

General procedure for the synthesis of 2-(5-bromo-1H-indol-3-yl)ethanol from methyl (5-bromo-1H-indol-3-yl)-acetate: to a solution of methyl ester (5-bromo-1H-indol-3-yl)-acetate (4 mmol, 1 eq.) in anhydrous THF (50 mL) was added lithium aluminum hydride (LiAlH4; 16 mmol, 4 eq.) in batches and the reaction The temperature was maintained at 0 °C. The reaction mixture was gradually brought to room temperature with continuous stirring for 30 min. The excess LiAlH4 was quenched by slow addition of saturated aqueous Na2SO4 while maintaining the temperature at about 0 °C. The reaction mixture was filtered. The reaction mixture was filtered and the filtrate was washed with THF. After combining the filtrates, the solvent was removed by concentration under reduced pressure and the residue was adjusted to pH 6 with 10% HCl solution and subsequently extracted with CHCl3. The organic layers were combined, dried with anhydrous Na2SO4, filtered and evaporated to dryness. The crude product was purified by fast column chromatography using EtOAc/hexane as eluent to afford the target product 2-(5-bromo-1H-indol-3-yl)ethanol. Yield: 83%; 1H NMR (300 MHz, CDCl3): δ 2.97 (t, J = 18 Hz, 2H), 3.86-3.93 (m, 2H), 4.09 (t, J = 21 Hz, 1H), 7.09 (d, J = 3 Hz, 1H), 7.22 (d, J = 9 Hz, 1H), 7.75 (s, 1H), 8.10 ( s, 1H); MS (APCI): m/z 241.2 [M + H]+.

References

[1] Journal of Medicinal Chemistry, 2010, vol. 53, # 19, p. 6838 - 6850
[2] Patent: WO2011/14128, 2011, A1. Location in patent: Page/Page column 65

5-BromotryptopholSupplier

TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Email
Sales-CN@TCIchemicals.com
Wuhan Chemwish Technology Co., Ltd
Tel
86-027-67849912
Email
sales@chemwish.com
Capot Chemical Co., Ltd
Tel
+86 (0) 571 85 58 67 18
Shanghai Longsheng chemical Co.,Ltd.
Tel
021-58099652-8005 13585536065
Email
bin.wu@shlschem.com
Shandong Xiya Chemical Co., Ltd
Tel
4009903999 13355009207
Email
3007715519@qq.com