Acetyl bromide → 1-Acetyl-3-hydroxypyrid-2-one

HRID 1871785Notes

Reaction equation

HRID 1871785 reaction equation
[OH:1][C:2]1[C:7]([OH:8])=[CH:6][CH:5]=[CH:4][N:3]=1.[C:9](Br)(=[O:11])[CH3:10]>O>[C:9]([N:3]1[CH:4]=[CH:5][CH:6]=[C:7]([OH:8])[C:2]1=[O:1])(=[O:11])[CH3:10]

Participants

4

Procedure

2,3-Dihydroxypyridine (5.55 g) is refluxed with acetylbromide (10 ml) overnight. The reaction mixture is allowed to cool and water (10 ml) is added. The resulting suspension is extracted with methylene chloride and the methylene chloride solution is dried over Na2SO4 and evaporated. The resultant residue is recrystallised from petroleum ether (80°-100° C.) to give 1-acetyl-3-hydroxypyrid-2-one as white crystals (2.8 g), m.p. 140°-141° C.; νmax (nujol) 1680, 3120 cm-1 ; δ(d6DMSO), 2.2 (s, 3H), 6.1 (t, 1H), 6.65 (m, 1H), 7.2 (d, 1H).

Workup

  1. temperatureto cool
  2. extractionThe resulting suspension is extracted with methylene chloride
  3. dry with materialthe methylene chloride solution is dried over Na2SO4
  4. customevaporated
  5. customThe resultant residue is recrystallised from petroleum ether (80°-100° C.)

Sources & evidence

ORD record
ord-e4ca0c3e08964a5b9c819985fe09a4a7
Source dataset
uspto-grants-2000_08
Patent number
USRE036831

Reaction notes

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