Acetic Acid → HCID 13957658, compound

HRID 1761340Notes

Reaction equation

HRID 1761340 reaction equation
C(O)(=O)C.[F:5][C:6]([F:29])([F:28])[C:7]1[NH:8][C:9]([C:24]([F:27])([F:26])[F:25])=[C:10]([C:19]([O:21][CH2:22][CH3:23])=[O:20])[CH:11]([CH3:18])[C:12]=1[C:13]([O:15][CH2:16][CH3:17])=[O:14].N([O-])=O.[Na+]>O>[F:29][C:6]([F:5])([F:28])[C:7]1[C:12]([C:13]([O:15][CH2:16][CH3:17])=[O:14])=[C:11]([CH3:18])[C:10]([C:19]([O:21][CH2:22][CH3:23])=[O:20])=[C:9]([C:24]([F:25])([F:27])[F:26])[N:8]=1

Participants

5

Reactant 3

HCID 176Acetic AcidHCID 13957627HCID 13957627, compoundHCID 23668193Sodium Nitrite

Product 1

HCID 13957658HCID 13957658, compoundYield 43.5%

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

A 50 ml round bottomed flask is charged with 20 ml of glacial acetic acid. To this is added 5 g (0.0133 mole) of diethyl 2,6-bis(trifluoromethyl)-4-methyl-1,4-dihydro-3,5-pyridinedicarboxylate, followed by a slow addition of 3 g (0.0434 mole) of sodium nitrite. The flask is immediately fitted with a condenser and nitrogen line, the stirring continued for 18 hours, and the mixture is poured over crushed ice and water. The organics are extracted twice with ether, washed once with saturated aqueous sodium chloride and washed twice with saturated aqueous sodium bicarbonate solution. The organics are dried over anhydrous magnesium sulfate and concentrated yielding 2.16 g (43.5%) of product, m.p. 55°-58° C.

Workup

  1. customThe flask is immediately fitted with a condenser
  2. additionthe mixture is poured
  3. extractionThe organics are extracted twice with ether
  4. washwashed once with saturated aqueous sodium chloride
  5. washwashed twice with saturated aqueous sodium bicarbonate solution
  6. dry with materialThe organics are dried over anhydrous magnesium sulfate
  7. concentrationconcentrated

Sources & evidence

ORD record
ord-c3bf5b7e3509421e96898eda90b27c1c
Source dataset
uspto-grants-1989_05
Patent number
US04826530

Reaction notes

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