(6-Chloro-2-pyridinyl)methanol
(6-Chloro-2-pyridinyl)methanol Basic information
- Product Name:
- (6-Chloro-2-pyridinyl)methanol
- Synonyms:
-
- CHEMPACIFIC 38159
- (6-CHLORO-PYRIDIN-2-YL)-METHANOL
- (6-Chloro-2-pyridinyl)methanol
- 2-Chloro-6-(Hydroxymethyl)Pyridine
- 6-Chloro-2-pyridinemethanol
- 2-Chloropyridine-6-Methanol
- 2-Pyridinemethanol, 6-chloro-
- (6-Chloro-2-pyridinyl)methanol ISO 9001:2015 REACH
- CAS:
- 33674-97-4
- MF:
- C6H6ClNO
- MW:
- 143.57
- EINECS:
- 807-010-1
- Mol File:
- 33674-97-4.mol
(6-Chloro-2-pyridinyl)methanol Chemical Properties
- Boiling point:
- 251.8±25.0 °C(Predicted)
- Density
- 1.324±0.06 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- pka
- 13.12±0.10(Predicted)
- form
- liquid
- color
- Colourless
(6-Chloro-2-pyridinyl)methanol Usage And Synthesis
Synthesis
6636-55-1
33674-97-4
General procedure for the synthesis of 2-chloro-6-hydroxymethylpyridine from methyl 6-chloropyridine-2-carboxylate: 6.7 g (39.0 mmol) of methyl 6-chloropyridine-2-carboxylate was dissolved in 90 mL of anhydrous tetrahydrofuran, which was subsequently cooled to -45 °C. A 40 mL solution of 1 M lithium aluminum hydride in tetrahydrofuran was added slowly and dropwise over 30 min. The reaction mixture was stirred at -45°C for 30 minutes and then slowly warmed to 0°C and continued stirring for 30 minutes. Subsequently, 15 mL of 1 N aqueous sodium hydroxide solution was slowly added dropwise to quench the reaction. Solid impurities were removed by diatomaceous earth filtration and the filtrate was concentrated to give 5.08 g (35.4 mmol, 91% yield) of 2-chloro-6-hydroxymethylpyridine. The product was characterized by 1H NMR (CDCl3, ppm): δ 7.61 (1H, d), 7.30 (1H, t), 7.04 (1H, d), 3.72 (2H, s).FAB MS (m/z) = 144 [M + 1].
References
[1] Patent: WO2007/58482, 2007, A1. Location in patent: Page/Page column 47-48
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(6-Chloro-2-pyridinyl)methanol(33674-97-4)Related Product Information
- 6-Chloropicolinic acid
- Picloram
- Tetrachloropyridine-2-carboxylic acid
- Clopyralid (2-hydroxyethyl)ammonium
- PICLORAM METHYL ESTER
- Clopyralid
- 6-CHLORO-2-PICOLINIC ACID METHYL ESTER
- CLOPYRALID METHYL ESTER
- (5-Chloro-3-pyridinyl)methanol
- (2-CHLORO-3-PYRIDINYL)METHANOL
- (4-Chloro-3-pyridinyl)methanol
- (2-CHLORO-4-PYRIDINYL)METHANOL
- (4-chloro-2-pyridinyl)methanol
- 6-CHLORO-2-HYDROXYMETHYL PYRIDINE HYDROCHLORIDE
- (6-CHLORO-3-PYRIDINYL)METHANOL
- 2,5-DICHLORO-3-HYDROXYMETHYLPYRIDINE
- ETHYL 3,4,5,6-TETRACHLOROPYRIDINE-2-CARBOXYLATE
- 2-Pyridinecarboxylic acid, 4-amino-3,5,6-trichloro-, isooctyl ester