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4-Bromobutyronitrile → 4-(5-Methyl-4-imidazolylmethylthio)butyronitrile

HRID 1382765
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HRID 1382765 반응식
[Na].[CH3:2][C:3]1[NH:7][CH:6]=[N:5][C:4]=1[CH2:8][SH:9].Br[CH2:11][CH2:12][CH2:13][C:14]#[N:15]>C(O)C>[CH3:2][C:3]1[NH:7][CH:6]=[N:5][C:4]=1[CH2:8][S:9][CH2:11][CH2:12][CH2:13][C:14]#[N:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 214124-BromobutyronitrileHCID 5360545SodiumHCID 13373992(5-Methyl-1H-imidazol-4-yl)methanethiol

생성물 1

HCID 212732904-(5-Methyl-4-imidazolylmethylthio)butyronitrile

시약·촉매·용매 1

HCID 702Ethanol용매2회

실험 절차

Sodium (5.0 g) was dissolved in ethanol (300 ml) and 5-methyl-4-(mercaptomethyl)imidazole (17 g) added, followed by a solution of 4-bromobutyronitrile (16 g) in ethanol (50 ml). The mixture was stirred under reflux for 45 minutes, cooled, filtered and the filtrate evaporated to dryness. The residue was taken up in water and extracted with ethyl acetate. The extract was dried (MgSO4) and solvent removed. Recrystallisation of the product from ethanol-ether gave 4-(5-methyl-4-imidazolylmethylthio)butyronitrile as its hydrochloride salt (12 g).

후처리

  1. temperatureunder reflux for 45 minutes
  2. temperaturecooled
  3. filtrationfiltered
  4. customthe filtrate evaporated to dryness
  5. extractionextracted with ethyl acetate
  6. dry with materialThe extract was dried (MgSO4) and solvent
  7. customremoved
  8. customRecrystallisation of the product from ethanol-ether

출처 및 근거

ORD 기록
ord-230baa72ed0249c6a3803a7cfa090eb6
출처 데이터셋
uspto-grants-1989_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04808589

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