Water → HCID 67397893, 화합물

HRID 869675노트

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HRID 869675 반응식
CC(C)([O-])C.[K+].[CH3:7][C:8]1[C:9]([C:18]([O:20]CC)=O)=[N:10][C:11]2[C:16]([N:17]=1)=[CH:15][CH:14]=[CH:13][CH:12]=2.[C:23](#[N:25])[CH3:24].O>C1(C)C=CC=CC=1>[CH3:7][C:8]1[C:9]([C:18](=[O:20])[CH2:24][C:23]#[N:25])=[N:10][C:11]2[C:16]([N:17]=1)=[CH:15][CH:14]=[CH:13][CH:12]=2

참가 물질

6

반응물 4

HCID 962WaterHCID 6342AcetonitrileHCID 589024Ethyl 3-methylquinoxaline-2-carboxylateHCID 23665647Potassium tert-butoxide

생성물 1

HCID 67397893HCID 67397893, 화합물

시약·촉매·용매 1

HCID 1140Toluene용매2회

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온도
0 °C

실험 절차

To a suspension of potassium tert-butoxide (72.7 g, 647 mmol) in toluene (810 mL) was added a solution of ethyl 3-methylquinoxaline-2-carboxylate (70.0 g, 324 mmol) and acetonitrile (38.3 mL, 809 mmol) in toluene (270 mL) dropwise over 50 min at 5° C. After being stirred for 5 min at 0° C., water (585 mL) was added. The organic layer was extracted with water (100 mL) and the aqueous layer was combined and acidified to pH 3-4 with 10% aqueous hydrochloric acid. The resulting precipitate was collected and dissolved to tetrahydrofuran. And then the organic layer was dried over sodium sulfate, filtrated and concentrated in vacuo. The crude solid was purified by silica gel column chromatography (silica gel 2.2 kg, chloroform to chloroform:ethyl acetate=19:1) to give 3-(3-methylquinoxalin-2-yl)-3-oxopropanenitrile. MS (APCI): m/z 212 (M+H).

후처리

  1. extractionThe organic layer was extracted with water (100 mL)
  2. customThe resulting precipitate was collected
  3. dissolutiondissolved to tetrahydrofuran
  4. dry with materialAnd then the organic layer was dried over sodium sulfate
  5. filtrationfiltrated
  6. concentrationconcentrated in vacuo
  7. customThe crude solid was purified by silica gel column chromatography (silica gel 2.2 kg, chloroform to chloroform:ethyl acetate=19:1)

출처 및 근거

ORD 기록
ord-d421b106e8df4ae48f7a35dedf40c496
출처 데이터셋
uspto-grants-2015_03
특허 번호
US08969376B2

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