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

HRID 1938710
ノート
印刷プレビュー

反応式

HRID 1938710 の反応式
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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 6228Dimethylformamide2 回HCID 24813Phosphorus oxychlorideHCID 4257156ethyl 2-phenyl-2-(1H-pyrazol-1-yl)acetate

生成物 1

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

反応条件

温度
70 °C

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-d5bad1c5181d4f3d957233f744135c3d
出典データセット
uspto-grants-1997_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05693657

反応ノート

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