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Phosphorus oxychloride → 2,2-dimethyl-4-chloro-6-cyano-2H-1,3-benzoxazine

HRID 326579
ノート
印刷プレビュー

反応式

HRID 326579 の反応式
P(Cl)(Cl)([Cl:3])=O.[C:6]([C:8]1[CH:9]=[CH:10][C:11]2[O:16][C:15]([CH3:18])([CH3:17])[NH:14][C:13](=O)[C:12]=2[CH:20]=1)#[N:7]>CN(C)C=O>[Cl:3][C:13]1[C:12]2[CH:20]=[C:8]([C:6]#[N:7])[CH:9]=[CH:10][C:11]=2[O:16][C:15]([CH3:18])([CH3:17])[N:14]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 24813Phosphorus oxychlorideHCID 108219722,2-dimethyl-6-cyano-3,4-dihydro-2H-1,3-benzoxazin-4-one

生成物 1

HCID 147215882,2-dimethyl-4-chloro-6-cyano-2H-1,3-benzoxazine

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

Phosphorous oxychloride (0.5 ml) was added with ice-cooling to dimethylformamide (10 ml) and the mixture was stirred for 10 minutes. To the mixture was added 6-cyano-2,2-dimethyl-3,4-dihydro-2H-1,3-benzoxazin-4-one (1.0 g), and the mixture was stirred with ice-cooling for 1 hour and then at room temperature for 2 hours. The mixture was extracted with addition of ethyl acetate and ice water. The ethyl acetate layer was successively washed with an aqueous sodium bicarbonate solution and saturated saline, dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure. Hexane was added to the residue and 4-chloro-6-cyano-2,2-dimethyl-2H-1,3-benzoxazine (0.41 g, mp. 124°-126° C.) was obtained by crystallization therefrom.

後処理

  1. stirringthe mixture was stirred with ice-
  2. temperaturecooling for 1 hour
  3. waitat room temperature for 2 hours
  4. extractionThe mixture was extracted with addition of ethyl acetate and ice water
  5. washThe ethyl acetate layer was successively washed with an aqueous sodium bicarbonate solution and saturated saline
  6. dry with materialdried over anhydrous magnesium sulfate
  7. distillationThe solvent was distilled off under reduced pressure
  8. additionHexane was added to the residue

出典と根拠

ORDレコード
ord-59f07b0f946f4f9e8d5e7ab10ad12c4b
出典データセット
uspto-grants-1993_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05270308

反応ノート

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