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Chemical Structure| 74650-71-8 Chemical Structure| 74650-71-8

Structure of 74650-71-8

Chemical Structure| 74650-71-8

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Product Details of [ 74650-71-8 ]

CAS No. :74650-71-8
Formula : C7H6ClNO3
M.W : 187.58
SMILES Code : COC1=CN=C(Cl)C(=C1)C(O)=O
MDL No. :MFCD16610607

Safety of [ 74650-71-8 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 74650-71-8 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 74650-71-8 ]

[ 74650-71-8 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 74650-70-7 ]
  • [ 74650-71-8 ]
  • 2
  • [ 74650-71-8 ]
  • [ 74650-73-0 ]
  • 3
  • [ 7732-18-5 ]
  • [ 74650-70-7 ]
  • [ 74650-71-8 ]
YieldReaction ConditionsOperation in experiment
1.6 g (35%) With potassium permanganate; (C) Preparation of 2-chloro-5-methoxynicotinic Acid A mixture of <strong>[74650-70-7]2-chloro-5-methoxy-3-methylpyridine</strong> (5.0 g, 0.031 mol), H2 O (400 mL) and KMnO4 (18.8 g, 0.12 mol) was heated at reflux for 1 hour. The resulting mixture was then filtered hot through super-cel, cooled and extracted with CH2 Cl2 (3*). The organic layer was dried, filtered and concentrated to yield 1.1 g of recovered <strong>[74650-70-7]2-chloro-5-methoxy-3-methylpyridine</strong>. The aqueous layer was acidified with 12 N HCl concentrated to a small volume. The solid filtered recrystallized from iso-PrOH/Et2 O to yield 1.6 g (35%) of 2-chloro-5-methoxynicotinic acid, mp 169-70 C.; 1 H NMR (DMSO-d6) delta3.95 (3H, s), 7.85 (1H, d, J=3) and 8.3 (1H, d, J=3); IR (nujol) 1740 cm-1.
1.6 g (35%) With potassium permanganate; (C) Preparation of 2-chloro-5-methoxynicotinic Acid A mixture of <strong>[74650-70-7]2-chloro-5-methoxy-3-methylpyridine</strong> (5.0 g, 0.031 mol), H2 O (400 mL) and KMnO4 (18.8 g, 0.12 mol) was heated at reflux for 1 hour. The resulting mixture was then filtered hot through super-cel, cooled and extracted with CH2 Cl2 (3X). The organic layer was dried, filtered and concentrated to yield 1.1 g of recovered <strong>[74650-70-7]2-chloro-5-methoxy-3-methylpyridine</strong>. The aqueous layer was acidified with 12 N HCl concentrated to a small volume. The solid filtered recrystallized from iso-PrOH/Et2 O to yield 1.6 g (35%) of 2-chloro-5-methoxynicotinic acid, mp 169-70 C.; 1 H NMR (DMSO-d6) delta 3.95 (3H, s), 7.85 (1H, d, J=3) and 8.3 (1H, d, J=3); IR (nujol) 1740 cm-1.
 

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