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Water → HCID 86647413, 화합물

HRID 2070945
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인쇄 미리보기

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HRID 2070945 반응식
Cl[CH2:2][C:3]1[C:4]([CH3:13])=[N:5][C:6]([CH3:12])=[C:7]([C:9]([CH3:11])=[CH2:10])[CH:8]=1.[N-:14]=[N+:15]=[N-:16].[Na+].O.CCOC(C)=O>CN(C=O)C>[N:14]([CH2:2][C:3]1[C:4]([CH3:13])=[N:5][C:6]([CH3:12])=[C:7]([C:9]([CH3:11])=[CH2:10])[CH:8]=1)=[N+:15]=[N-:16]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 8857Ethyl AcetateHCID 33557Sodium AzideHCID 68670764HCID 68670764, 화합물

생성물 1

HCID 86647413HCID 86647413, 화합물

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
70 °C

실험 절차

A mixture of 96.5 mg of the 3-(chloromethyl)-2,6-dimethyl-5-(prop-1-en-2-yl)pyridine and 86.8 mg (1.34 mmol) of NaN3 in 3 mL of DMF was heated at 70° C. for 4 h. Water and EtOAc were added, and the layers were separated. The organic layer was washed with H2O (2×) and then with brine. It was dried over Na2SO4, filtered, and concentrated to give the crude azide (3-(azidomethyl)-2,6-dimethyl-5-(prop-1-en-2-yl)pyridine) which was used without further purification.

후처리

  1. customthe layers were separated
  2. washThe organic layer was washed with H2O (2×)
  3. dry with materialIt was dried over Na2SO4
  4. filtrationfiltered
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-435f5a11b9c54a84ae187c5b90f43d93
출처 데이터셋
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08299267B2

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