Basic information Safety Supplier Related

3-(BROMOMETHYL)PHENOL

Basic information Safety Supplier Related

3-(BROMOMETHYL)PHENOL Basic information

Product Name:
3-(BROMOMETHYL)PHENOL
Synonyms:
  • 3-(BROMOMETHYL)PHENOL
  • AKOS 90890
  • 3-Hydroxybenzylbromide
  • m-(Bromomethyl)phenol
  • Phenol, 3-(bromomethyl)-
  • 6-Quinolinesulfonylchloride,1,2-dihydro-4-oxo-
  • 3-(Bromomethyl)phenol CAS NO.74597-04-9
CAS:
74597-04-9
MF:
C7H7BrO
MW:
187.03
Mol File:
74597-04-9.mol
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3-(BROMOMETHYL)PHENOL Chemical Properties

Boiling point:
272℃
Density 
1.593
Flash point:
118℃
storage temp. 
Inert atmosphere,Store in freezer, under -20°C
pka
9.55±0.10(Predicted)
Appearance
White to off-white Solid
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Safety Information

RIDADR 
2810
HazardClass 
6.1
PackingGroup 
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3-(BROMOMETHYL)PHENOL Usage And Synthesis

Uses

3-?(Bromomethyl)?phenol is a reagent used in synthesis of furan-based heterocycles. Also used in the preparation of tetrahydroisoquinolinyl triazole carboxamide and triazole substituted benzamide analogues as σ2 receptors.

Synthesis

620-24-6

74597-04-9

General procedure for the synthesis of m-hydroxybenzyl bromide from 3-hydroxybenzyl alcohol: Synthesis of Intermediate 17: 3-(bromomethyl)phenol A 50 mL round bottom flask was charged with 15 mL of dichloromethane and fitted with a magnetic stirrer. To the stirred solvent was added 3-hydroxymethylphenol (0.5 g, 4.03 mmol). After cooling the reaction mixture to 0°C, phosphorus tribromide (1.6 g, 0.56 mL, 6.04 mmol) was added dropwise. After the dropwise addition, the reaction mixture was stirred at room temperature for 1 hour. After the reaction was completed, the reaction mixture was diluted with 25 mL of dichloromethane and the organic layer was washed with 20 mL of water. The organic layer was dried with anhydrous Na2SO4 and concentrated under reduced pressure to remove the solvent to give a brown solid product (0.65 g, yield: 86.3%). Mass spectrum (ESI, 120 eV): m/z = 187.0 (M + H)+. 1H NMR (300MHz, CDCl3): δ 7.10-7.15 (t, 1H), 6.86-6.89 (d, 1H), 6.80 (d, 1H), 6.67-6.71 (m, 1H), 4.35-4.36 (d, 2H), 3.80-3.94 (broad peak, 1H).

References

[1] Chemische Berichte, 1989, vol. 122, p. 347 - 356
[2] Patent: WO2012/11125, 2012, A1. Location in patent: Page/Page column 70; 71-72
[3] Patent: WO2014/31936, 2014, A2. Location in patent: Paragraph 0327; 0328
[4] Patent: WO2014/31928, 2014, A2. Location in patent: Paragraph 0334
[5] Patent: WO2005/68421, 2005, A1. Location in patent: Page/Page column 39-40

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