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

HRID 259671
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HRID 259671 반응식
[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
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참가 물질

7

반응물 4

HCID 313Hydrochloric AcidHCID 11430Potassium CarbonateHCID 95576Methyl 2-bromopropionateHCID 178518989HCID 178518989, 화합물

생성물 1

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

시약·촉매·용매 2

HCID 962Water용매
HCID 6228
Dimethylformamide
용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-1351e68b91114a0cab228058f3c14150
출처 데이터셋
uspto-grants-1996_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05523278

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