5-CHLORO-2-HYDROXYBENZONITRILE
5-CHLORO-2-HYDROXYBENZONITRILE Basic information
- Product Name:
- 5-CHLORO-2-HYDROXYBENZONITRILE
- Synonyms:
-
- Benzonitrile, 5-chloro-2-hydroxy-
- 2-Hydroxy-5-chlorobenzonitrile
- 5-Chlorosalicylonitrile
- 5-CHLORO-2-HYDROXYBENZONITRILE
- AKOS B029245
- 5-Chloro-2-hydroxybenzonitrile, tech
- 4-Chloro-2-cyanophenol
- 4-Chloro-2-cyanophenol, 5-Chlorosalicylonitrile
- CAS:
- 13589-72-5
- MF:
- C7H4ClNO
- MW:
- 153.57
- Product Categories:
-
- Aromatic Nitriles
- Phenyls & Phenyl-Het
- Phenyls & Phenyl-Het
- Mol File:
- 13589-72-5.mol
5-CHLORO-2-HYDROXYBENZONITRILE Chemical Properties
- Melting point:
- 152-154°C
- Boiling point:
- 269.4±25.0 °C(Predicted)
- Density
- 1.41±0.1 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- pka
- 6.72±0.18(Predicted)
- Appearance
- Light brown to off-white Solid
- CAS DataBase Reference
- 13589-72-5(CAS DataBase Reference)
Safety Information
- Hazard Codes
- Xi
- Risk Statements
- 20/21/22-36/37/38-36
- Safety Statements
- 26-36/37/39
- RIDADR
- 3276
- HS Code
- 2926907090
5-CHLORO-2-HYDROXYBENZONITRILE Usage And Synthesis
Synthesis
635-93-8
13589-72-5
The general procedure for the synthesis of 5-chloro-2-hydroxybenzonitrile from 5-chlorosalicylaldehyde is as follows: 1. 5-Chloro-2-hydroxybenzaldehyde (300 g, 1.92 mol) was suspended in water (4.5 L) with hydroxylamine-O-sulfonic acid (260 g, 2.30 mol) at room temperature. 2. The reaction mixture was stirred at 60 °C for 7 hours. 3. Upon completion of the reaction, water (3 L) was added to the mixture, which was subsequently chilled with ice. 4. The precipitated crystals were collected by filtration and washed with 1.5 L of water. 5. The resulting crystals were re-suspended in 1.5 L of water, filtered and washed with water. 6. 6. Finally, the crystals were tray dried at 50 °C for 22 h to give 272 g of 5-chloro-2-hydroxybenzonitrile (white crystals, yield: 93%). The structure of the product was confirmed by 1H-NMR (CDCl3): δ 6.94 (1H, d, J = 8.8 Hz), 7.42 (1H, dd, J = 8.8,2.9 Hz), 7.47 (1H, d, J = 2.9 Hz).
References
[1] Patent: WO2006/115130, 2006, A1. Location in patent: Page/Page column 53-54
[2] Patent: US2007/117866, 2007, A1
[3] Gazzetta Chimica Italiana, 1959, vol. 89, p. 1009,1013
[4] Journal of Molecular Recognition, 2012, vol. 25, # 6, p. 352 - 360
[5] Journal of Organic Chemistry, 2015, vol. 80, # 2, p. 1229 - 1234
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5-CHLORO-2-HYDROXYBENZONITRILE(13589-72-5)Related Product Information
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