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Dimethylformamide → ethyl (+/-)-4-formyl-alpha-phenyl-1H-pyrazole-l-acetate

HRID 1938710
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HRID 1938710 반응식
P(Cl)(Cl)(Cl)=O.[C:6]1([CH:12]([N:18]2[CH:22]=[CH:21][CH:20]=[N:19]2)[C:13]([O:15][CH2:16][CH3:17])=[O:14])[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1.CN([CH:26]=[O:27])C>>[CH:26]([C:21]1[CH:20]=[N:19][N:18]([CH:12]([C:6]2[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=2)[C:13]([O:15][CH2:16][CH3:17])=[O:14])[CH:22]=1)=[O:27]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 6228Dimethylformamide2회HCID 24813Phosphorus oxychlorideHCID 4257156ethyl 2-phenyl-2-(1H-pyrazol-1-yl)acetate

생성물 1

HCID 10563150ethyl (+/-)-4-formyl-alpha-phenyl-1H-pyrazole-l-acetate수율 89%

반응 조건

온도
70 °C

실험 절차

Phosphorous oxychloride (7.0 mL, 75 mmol) was added dropwise to 14 mL DMF at 0° C. under an atmosphere of N2. The resulting solution was stirred for 0.5 hour and then a solution of ethyl (±)-α-phenyl-1H-pyrazole-1-acetate (5.76 g, 25 mmol) in 5 mL DMF was added dropwise. The resulting orange solution was warmed to 70° C. for 16 hours. The reaction mixture was cooled to 0° C. and carefully quenched with saturated Na2CO3 solution. The reaction mixture was partitioned between water and ether and the ether layer was dried over MgSO4, filtered, and concentrated to give an orange oil. Chromatography (15% EtOAc/hexanes on silica) gave 5.73 g (89%) of the title compound as a yellow/green oil which solidified upon standing; mp 68°-70° C.

후처리

  1. temperatureThe reaction mixture was cooled to 0° C.
  2. customcarefully quenched with saturated Na2CO3 solution
  3. customThe reaction mixture was partitioned between water and ether
  4. dry with materialthe ether layer was dried over MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customto give an orange oil

출처 및 근거

ORD 기록
ord-d5bad1c5181d4f3d957233f744135c3d
출처 데이터셋
uspto-grants-1997_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05693657

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