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Sodium Azide → (E)-4-(4-azidobut-1-enyl)-1,2-dichlorobenzene

HRID 1771087
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HRID 1771087 반응식
CS(O[CH2:6][CH2:7]/[CH:8]=[CH:9]/[C:10]1[CH:15]=[CH:14][C:13]([Cl:16])=[C:12]([Cl:17])[CH:11]=1)(=O)=O.[N-:18]=[N+:19]=[N-:20].[Na+]>CN(C=O)C.CCOC(C)=O>[N:18]([CH2:6][CH2:7]/[CH:8]=[CH:9]/[C:10]1[CH:15]=[CH:14][C:13]([Cl:16])=[C:12]([Cl:17])[CH:11]=1)=[N+:19]=[N-:20]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 33557Sodium AzideHCID 86728171(E)-4-(3,4-dichlorophenyl)but-3-enyl methanesulfonate

생성물 1

HCID 86728172(E)-4-(4-azidobut-1-enyl)-1,2-dichlorobenzene수율 87%

시약·촉매·용매 2

HCID 6228Dimethylformamide용매HCID 8857Ethyl Acetate용매

실험 절차

To a solution of Intermediate 2C (1.3 g, 4.4 mmol) in DMF (7 mL) was added NaN3 (0.86 g, 13 mmol). The reaction mixture was stirred at rt for 16 h. The reaction mixture was diluted with EtOAc (100 mL). The organic layer was washed with 10% aqueous LiCl solution (3×200 mL), dried over Na2SO4 and dried in vacuo. The product was isolated by silica gel chromatography to obtain 570 mg (87% yield) of Intermediate 2D. HPLC/MS (Method C) RT=4.02 min, [M+Na]+ 263.2.

후처리

  1. washThe organic layer was washed with 10% aqueous LiCl solution (3×200 mL)
  2. dry with materialdried over Na2SO4
  3. customdried in vacuo
  4. customThe product was isolated by silica gel chromatography

출처 및 근거

ORD 기록
ord-a762d278308440e7ba60d976d6ea8c4f
출처 데이터셋
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09249096B2

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