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Iodoethane → HCID 66986289, 화합물

HRID 555992
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HRID 555992 반응식
[C:1]([O:5][C:6](=[O:14])[NH:7][CH2:8][C:9]1[N:10]=[N:11][NH:12][N:13]=1)([CH3:4])([CH3:3])[CH3:2].[H-].[Na+].[CH2:17](I)[CH3:18]>CN(C=O)C>[C:1]([O:5][C:6](=[O:14])[NH:7][CH2:8][C:9]1[N:10]=[N:11][N:12]([CH2:17][CH3:18])[N:13]=1)([CH3:4])([CH3:2])[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6340IodoethaneHCID 24758Sodium hydrideHCID 20043629tert-Butyl (2H-tetrazol-5-ylmethyl)carbamate

생성물 1

HCID 66986289HCID 66986289, 화합물

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

(2H-Tetrazol-5-ylmethyl)-carbamic acid tert-butyl ester (0.9 g, 4.5 mmol) is dissolved in dry DMF, NaH (60% dispersed in mineral oil) (0.18 g, 4.5 mmol) is added and the reaction mixture is stirred at room temperature for 5 minutes before ethyl iodide (0.35 ml, 4.5 mmol) is added. The reaction mixture is stirred overnight at room temperature and partitioned between EtOAc and water. The organic phase is dried over MgSO4, filtered and concentrated in vacuo to afford an oil. Purification by flash chromatography on silica eluting with 2:1 iso-hexanes/EtOAc affords the title compound.

후처리

  1. additionis added
  2. custompartitioned between EtOAc and water
  3. dry with materialThe organic phase is dried over MgSO4
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo
  6. customto afford an oil
  7. customPurification by flash chromatography on silica eluting with 2:1 iso-hexanes/EtOAc

출처 및 근거

ORD 기록
ord-1ed168d17cc84b029f311da8a95a9ac6
출처 데이터셋
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08053574B2

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