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Hydrochloric Acid → Methyl 2-[(6-chloro-1,2-benzisoxazol-3-yl)oxy]propionate

HRID 259671
ノート
印刷プレビュー

反応式

HRID 259671 の反応式
[Cl:1][C:2]1[CH:11]=[CH:10][C:5]2[C:6]([OH:9])=[N:7][O:8][C:4]=2[CH:3]=1.C(=O)([O-])[O-].[K+].[K+].Br[CH:19]([CH3:24])[C:20]([O:22][CH3:23])=[O:21].Cl>CN(C)C=O.O>[Cl:1][C:2]1[CH:11]=[CH:10][C:5]2[C:6]([O:9][CH:19]([CH3:24])[C:20]([O:22][CH3:23])=[O:21])=[N:7][O:8][C:4]=2[CH:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 313Hydrochloric AcidHCID 11430Potassium CarbonateHCID 95576Methyl 2-bromopropionateHCID 178518989HCID 178518989、化合物

生成物 1

HCID 22402920Methyl 2-[(6-chloro-1,2-benzisoxazol-3-yl)oxy]propionate

試薬・触媒・溶媒 2

HCID 962Water溶媒
HCID 6228
Dimethylformamide
溶媒

実験手順

A mixture of 6-chloro-1,2-benzisoxazol-3-ol (6.8 g, 40.1 mmol), potassium carbonate (8.3 g, 60 mmol) and methyl 2-bromopropionate (10.0 g, 60.1 mmol) in N,N-dimethylformamide is stirred at room temperature over-night and diluted with water. The resultant aqueous mixture is acidified with concentrated hydrochloric acid (pH5-pH6) and extracted with methylene chloride. The combined organic extracts are diluted with hexanes, washed with water, dried over anhydrous sodium sulfate and concentrated in vacuo to obtain a residue. Column chromatography of the residue using silica gel and ethyl acetate/hexanes solutions gives the title product as a gold oil which is identified by NMR spectral analyses.

後処理

  1. extractionextracted with methylene chloride
  2. additionThe combined organic extracts are diluted with hexanes
  3. washwashed with water
  4. dry with materialdried over anhydrous sodium sulfate
  5. concentrationconcentrated in vacuo
  6. customto obtain a residue

出典と根拠

ORDレコード
ord-1351e68b91114a0cab228058f3c14150
出典データセット
uspto-grants-1996_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05523278

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート