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Hydrochloric Acid → HCID 19786539、化合物

HRID 1196573
ノート
印刷プレビュー

反応式

HRID 1196573 の反応式
CN([CH2:4][N:5]([CH3:7])[CH3:6])C.FC(F)(F)C(O)=O.[C:15]1([C:21]2[C:25]3[C:26](=[O:30])[CH2:27][CH2:28][CH2:29][C:24]=3[O:23][N:22]=2)[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1.[ClH:31]>>[ClH:31].[CH3:7][N:5]([CH2:4][CH:27]1[C:26](=[O:30])[C:25]2[C:21]([C:15]3[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=3)=[N:22][O:23][C:24]=2[CH2:29][CH2:28]1)[CH3:6]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 4

HCID 313Hydrochloric Acid2 回HCID 5829N,N,N',N'-TetramethylmethanediamineHCID 6422Trifluoroacetic acidHCID 12344070HCID 12344070、化合物

生成物 1

HCID 19786539HCID 19786539、化合物

反応条件

温度
-10 °C

実験手順

Bis-dimethylaminomethane (0.51 g) was added to 2.5 ml of trifluoroacetic acid which had been previously chilled to -10° C. 6,7-Dihydro-3-phenyl-1,2-benzisoxazol-4(5H)-one (1.0 g) was then added and the reaction was warmed for 1 hour at 100° C. and then allowed to stand an additional 2 days at room temperature. The reaction mixture was poured into 5% HCl and washed with ether, after which the aqueous phase was treated with solid sodium bicarbonate until basic. Extraction with ether followed by drying and concentration gave an oil. The hydrochloride was formed in ethereal HCl and was recrystallized from dichloromethane/ether to give 0.95 g of 6,7-dihydro-5-dimethylaminomethyl-3-phenyl-1,2-benzisoxazol-4(5H)-one hydrochloride, m.p. 178°-180° C.

後処理

  1. temperaturethe reaction was warmed for 1 hour at 100° C.
  2. washwashed with ether
  3. additionafter which the aqueous phase was treated with solid sodium bicarbonate until basic
  4. extractionExtraction with ether
  5. customby drying
  6. concentrationconcentration
  7. customgave an oil

出典と根拠

ORDレコード
ord-821bbf20479b4318a32292710797a0c7
出典データセット
uspto-grants-1992_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05114936

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート