Chloroacetyl chloride → 6-Methoxy-3,4-dihydro-2H-1,4-benzoxazine

HRID 1167610ノート

反応式

HRID 1167610 の反応式
[NH2:1][C:2]1(O)C=CC(OC)=C[CH2:3]1.[C:11](=O)([O-])O.[Na+].Cl[CH2:17][C:18](Cl)=[O:19].[CH2:21]([C:25]([CH3:27])=[O:26])[CH:22](C)C>>[CH3:11][O:19][C:18]1[CH:22]=[CH:21][C:25]2[O:26][CH2:3][CH2:2][NH:1][C:27]=2[CH:17]=1

参加物

5

実験手順

The compound obtained in Step A (5.94 g; 42.7 mmol) is dissolved in 50 ml of methyl isobutyl ketone, and a solution of sodium hydrogen carbonate (3 eq.; 128.1 mmol; 10.76 g dissolved in 60 ml of water) is subsequently added. Chloroacetyl chloride (1.1 eq.; 46.9 mmol; 3.74 ml) is then slowly added. The mixture is maintained at reflux for one hour, then the methyl isobutyl ketone is removed under reduced pressure. The residue is taken up in ethyl acetate, and the organic phase is washed twice with water, dried over MgSO4, and subsequently removed under reduced pressure to yield the title product in the form of a solid.

後処理

  1. temperatureThe mixture is maintained
  2. temperatureat reflux for one hour
  3. customthe methyl isobutyl ketone is removed under reduced pressure
  4. washthe organic phase is washed twice with water
  5. dry with materialdried over MgSO4
  6. customsubsequently removed under reduced pressure

出典と根拠

ORDレコード
ord-c6432d1421b849cc93cbfc4aa75d3978
出典データセット
uspto-grants-2003_09
特許番号
US06620809B2

反応ノート

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