3-Bromobenzaldehyde → 2-(3-Bromophenyl)-4,5-dimethyloxazole-3-oxide

HRID 398107ノート

反応式

HRID 398107 の反応式
[CH3:1][C:2](=[N:6][OH:7])[C:3](=[O:5])[CH3:4].[Br:8][C:9]1[CH:10]=[C:11]([CH:14]=[CH:15][CH:16]=1)[CH:12]=O>C(O)(=O)C>[Br:8][C:9]1[CH:10]=[C:11]([C:12]2[O:5][C:3]([CH3:4])=[C:2]([CH3:1])[N+:6]=2[O-:7])[CH:14]=[CH:15][CH:16]=1

参加物

4

実験手順

A solution of 2,3-butanedione monooxime (50 g, 0.49 mol) and 3-bromobenzaldehyde (101 g, 0.54 mol) in acetic acid (500 mL) was cooled to 0° C. and then gaseous HCl was bubbled through the solution for 35 min while the reaction was stirred in an ice bath. Diethyl ether (500 mL) was then added to the reaction to precipitate the product and the resultant slurry stirred 45 min at 0° C. before being filtered. The solids were rinsed with Et2O (50 mL), taken up in water (1 L) and concentrated NH4OH (60 mL) added to the slurry. This mixture was extracted with CHCl3, the organic layer was dried (MgSO4), and the solvent removed in vacuo to give 97.4 g (74%) of 2-(3-bromophenyl)-4,5-dimethyloxazole-3-oxide as a white solid. The compound should be used directly with 24-48 h. 1H NMR (300 MHz, CDCl3) δ8.60 (s, 1H), 8.40 (d, J=8.0 Hz, 1H), 7.55 (d, J=8.0 Hz, 1H), 7.38 (d, J =8.0 Hz, 1H), 2.39 (s, 3H), 2.20 (s, 3H).

後処理

  1. customgaseous HCl was bubbled through the solution for 35 min while the reaction
  2. additionDiethyl ether (500 mL) was then added to the reaction
  3. customto precipitate the product
  4. stirringthe resultant slurry stirred 45 min at 0° C.
  5. filtrationbefore being filtered
  6. washThe solids were rinsed with Et2O (50 mL)
  7. additionconcentrated NH4OH (60 mL) added to the slurry
  8. extractionThis mixture was extracted with CHCl3
  9. dry with materialthe organic layer was dried (MgSO4)
  10. customthe solvent removed in vacuo

出典と根拠

ORDレコード
ord-1b3dc9fc2ab64e14a2f071aeeb42f541
出典データセット
uspto-grants-2003_08
特許番号
US06610696B2

反応ノート

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