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Sodium Cyanide → 5-(2-Propyl-3,4-dichlorophenoxy)pentane nitrile

HRID 34970
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HRID 34970 반응식
[CH2:1]([C:4]1[C:16]([Cl:17])=[C:15]([Cl:18])[CH:14]=[CH:13][C:5]=1[O:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11]Br)[CH2:2][CH3:3].[C-]#[N:20].[Na+]>CN(C)C=O>[CH2:1]([C:4]1[C:16]([Cl:17])=[C:15]([Cl:18])[CH:14]=[CH:13][C:5]=1[O:6][CH2:7][CH2:8][CH2:9][CH2:10][C:11]#[N:20])[CH2:2][CH3:3]
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참가 물질

4

반응물 2

HCID 8929Sodium CyanideHCID 212972695-(2-Propyl-3,4-dichlorophenoxy)pentyl bromide

생성물 1

HCID 212972585-(2-Propyl-3,4-dichlorophenoxy)pentane nitrile

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

A solution of 1.6 g. of 5-(2-propyl-3,4dichlorophenoxy)pentyl bromide and 0.22 g. of sodium cyanide were heated overnight at 75°-85° C. in 50 ml. of dimethylformamide. The solution was evaporated in vacuo and ethyl acetate and water were added to the residue. The layers were separated and the organic layer was washed several times with a saturated sodium chloride solution. The organic solution was filtered through sodium sulfate and evaporated to dryness to give 1.38 g. of the desired sub-title intermediate. NMR.

후처리

  1. customThe solution was evaporated in vacuo and ethyl acetate and water
  2. additionwere added to the residue
  3. customThe layers were separated
  4. washthe organic layer was washed several times with a saturated sodium chloride solution
  5. filtrationThe organic solution was filtered through sodium sulfate
  6. customevaporated to dryness
  7. customto give 1.38 g

출처 및 근거

ORD 기록
ord-b9adf9d7b096468f83a8b7ace2b09bac
출처 데이터셋
uspto-grants-1988_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04764521

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