1-methyl-4-nitro-1H-pyrazole → (Z)-1-(1-methyl-4-nitro-1H-pyrazol-5-yl)cyclohept-4-enol

HRID 521942

반응식

HRID 521942 반응식
[CH3:1][N:2]1[CH:6]=[C:5]([N+:7]([O-:9])=[O:8])[CH:4]=[N:3]1.[C:10]1(=[O:17])[CH2:16][CH2:15][CH:14]=[CH:13][CH2:12][CH2:11]1.C[Si](C)(C)[N-][Si](C)(C)C.[Li+].[Cl-].[NH4+]>C1COCC1>[CH3:1][N:2]1[C:6]([C:10]2([OH:17])[CH2:16][CH2:15][CH:14]=[CH:13][CH2:12][CH2:11]2)=[C:5]([N+:7]([O-:9])=[O:8])[CH:4]=[N:3]1

참가 물질

6

반응물 4

HCID 198951-methyl-4-nitro-1H-pyrazoleHCID 25517Ammonium ChlorideHCID 549335Cyclohept-4-en-1-oneHCID 2733832Lithium Hexamethyldisilazide

생성물 1

HCID 86680017(Z)-1-(1-methyl-4-nitro-1H-pyrazol-5-yl)cyclohept-4-enol수율 49%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

반응 조건

온도
-40 °C

실험 절차

To a solution of 1-methyl-4-nitro-1H-pyrazole (1.5 g, 11.8 mmol) and (Z)-cyclohept-4-enone (1.4 g, 13.0 mmol) in dry THF (30 mL) under nitrogen cooled to −78° C. was added dropwise a solution of lithium hexamethyldisilazide (1.0 M in THF, 30 mL, 29.5 mmol). The reaction mixture was allowed to warm to −40° C. and stirred for 90 min. Saturated aqueous ammonium chloride solution (30 mL) was added (dropwise initially) and the mixture was allowed to warm to room temperature and extracted with EtOAc (150 mL). The organic layer was washed with water (30 mL), washed with brine (20 mL), separated, dried over MgSO4 and concentrated under reduced pressure. Purification via silica gel column chromatography (20-25% EtOAc) gave (Z)-1-(1-methyl-4-nitro-1H-pyrazol-5-yl)cyclohept-4-enol as a tan oil (1.37 g, 49%).

후처리

  1. temperatureto warm to room temperature
  2. extractionextracted with EtOAc (150 mL)
  3. washThe organic layer was washed with water (30 mL)
  4. washwashed with brine (20 mL)
  5. customseparated
  6. dry with materialdried over MgSO4
  7. concentrationconcentrated under reduced pressure
  8. customPurification via silica gel column chromatography (20-25% EtOAc)

출처 및 근거

ORD 기록
ord-2fc1cce7738e49f3a797f537f2d6e4e8
출처 데이터셋
uspto-grants-2016_05
특허 번호
US09328106B2

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