Basic information Safety Supplier Related

7-Bromo-1-hydroxynaphthalene

Basic information Safety Supplier Related

7-Bromo-1-hydroxynaphthalene Basic information

Product Name:
7-Bromo-1-hydroxynaphthalene
Synonyms:
  • 7-Bromo-1-hydroxynaphthalene
  • 7-bromo-1-Naphthalenol
  • 7-Bromonaphthalen-1-ol
  • 1-Naphthalenol, 7-bromo-
  • 7-Bromo-1-naphthol
CAS:
91270-69-8
MF:
C10H7BrO
MW:
223.07
Mol File:
91270-69-8.mol
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7-Bromo-1-hydroxynaphthalene Chemical Properties

Boiling point:
353.8±15.0 °C(Predicted)
Density 
1.614±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
pka
8.93±0.40(Predicted)
Appearance
Off-white to pink Solid
InChI
InChI=1S/C10H7BrO/c11-8-5-4-7-2-1-3-10(12)9(7)6-8/h1-6,12H
InChIKey
STJXOXMPODAEAK-UHFFFAOYSA-N
SMILES
C1(O)=C2C(C=CC(Br)=C2)=CC=C1
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Safety Information

HS Code 
2908190090
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7-Bromo-1-hydroxynaphthalene Usage And Synthesis

Chemical Properties

white powder

Synthesis

32281-97-3

91270-69-8

Step D: A solution of tributylammonium tetrabromide (11.8 g, 24.4 mmol) in dichloromethane (80 mL) was slowly added dropwise to a mixture of dichloromethane (20 mL) and methanol (20 mL) of the product obtained in Step C (5.0 g, 22.2 mmol) at room temperature for a controlled period of more than 1 hour. After the dropwise addition, the reaction mixture was continued to be stirred at room temperature for 15 hours. After completion of the reaction, the mixture was concentrated. The concentrated residue was dissolved in dichloromethane and washed three times with saturated sodium bicarbonate solution. The organic layer was separated and concentrated and the residue was dissolved in dimethylformamide (100 mL). Subsequently, lithium carbonate (5.3 g, 71.1 mmol) and lithium bromide (4.1 g, 46.6 mmol) were added to the solution, and the reaction mixture was stirred at 140 °C for 1.5 hours. At the end of the reaction, it was cooled to room temperature, the solid was collected by filtration and washed with ethyl acetate. The filtrates were combined, washed four times with water and dried over anhydrous sodium sulfate to give the final 7-bromonaphthalen-1-ol (2.7 g, 56% yield). The product was characterized by 1H NMR (300 MHz, CDCl3): δ 8.41 (d, J = 1.8 Hz, 1H), 7.68 (d, J = 8.7 Hz, 1H), 7.57 (dd, J = 8.7, 1.8 Hz, 1H), 7.41 (d, J = 8.4 Hz, 1H), 7.28-7.35 (m, 1H), 6.62 (d J = 7.2 Hz, 1H), 5.80 (br s, 1H).

References

[1] Patent: US2006/52378, 2006, A1. Location in patent: Page/Page column 113
[2] ACS Medicinal Chemistry Letters, 2015, vol. 6, # 12, p. 1199 - 1203

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