Sodium Bicarbonate → HCID 14479958, compound

HRID 1029847Notes

Reaction equation

HRID 1029847 reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[O:10][C:11]([CH3:25])=[C:12]([CH2:14][O:15][C:16]3[CH:21]=[CH:20][CH:19]=[C:18]([N+:22]([O-])=O)[CH:17]=3)[N:13]=2)=[CH:5][CH:4]=1.C(=O)(O)[O-].[Na+]>C(O)C>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([C:9]2[O:10][C:11]([CH3:25])=[C:12]([CH2:14][O:15][C:16]3[CH:17]=[C:18]([NH2:22])[CH:19]=[CH:20][CH:21]=3)[N:13]=2)=[CH:7][CH:8]=1

Participants

4

Procedure

A solution of 6.0 g (0.18 mol) of 2-(4-methoxyphenyl)-5-methyl-4-[(3-nitrophenoxy)methyl]oxazole and 20.0 g (0.09 mol) of stannous chloride dihydrate in 150 ml of ethanol is heated to 70° C. for 20 hours. The solution is allowed to cool to room temperature and poured into 2 L of ice water. The mixture is made alkaline by the addition of solid sodium bicarbonate and extracted twice with 500 ml of ethyl acetate. The combined ethyl acetate solution is washed with 500 ml of brine, dried over anhydrous magnesium sulfate and concentrated in vacuo to obtain a residue. Recrystallization from ether/hexane gives 3.8 g (69%) of crystals, m.p. 132°-134° C. The product is used without further purification in subsequent reactions.

Workup

  1. extractionextracted twice with 500 ml of ethyl acetate
  2. washThe combined ethyl acetate solution is washed with 500 ml of brine
  3. dry with materialdried over anhydrous magnesium sulfate
  4. concentrationconcentrated in vacuo
  5. customto obtain a residue
  6. customRecrystallization from ether/hexane

Sources & evidence

ORD record
ord-7175851bb57646aabf52815b9a29c954
Source dataset
uspto-grants-1992_04
Patent number
US05103014

Reaction notes

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