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Methanesulfonic Acid → Ethyl 3-difluoromethyl-1-methyl-4-pyrazole carboxylate

HRID 1042958
ノート
印刷プレビュー

反応式

HRID 1042958 の反応式
[F:1][CH:2]([F:14])[C:3]1[N:7](C)[N:6]=[CH:5][C:4]=1[C:9]([O:11][CH2:12][CH3:13])=[O:10].P([O-])(OC)O[CH3:17].CS(O)(=O)=O>>[F:1][CH:2]([F:14])[C:3]1[C:4]([C:9]([O:11][CH2:12][CH3:13])=[O:10])=[CH:5][N:6]([CH3:17])[N:7]=1
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 6395Methanesulfonic AcidHCID 21884954DimethylphosphiteHCID 45933751Ethyl 5-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylate

生成物 1

HCID 11644126Ethyl 3-difluoromethyl-1-methyl-4-pyrazole carboxylate収率 69.1%

反応条件

温度
170 °C

実験手順

To 20.4 g of ethyl 5-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylate (iso-DFPE) was added 11.3 g of dimethyl phosphite and 0.82 g of methane sulfonic acid. The mixture was heated to 170° C. and stirred for 7 hours. The solution was cooled and distilled to recover recycled trimethyl phosphate and 0.9 g of starting ethyl 5-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylate (iso-DFPE). The remaining solution was added to 50 g of cold water. The solution was allowed to stir for 30 min. The precipitating solid was filtered and dried to give 14.1 g of product.

後処理

  1. temperatureThe solution was cooled
  2. distillationdistilled
  3. customto recover recycled trimethyl phosphate and 0.9 g of starting ethyl 5-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylate (iso-DFPE)
  4. additionThe remaining solution was added to 50 g of cold water
  5. stirringto stir for 30 min
  6. filtrationThe precipitating solid was filtered
  7. customdried

出典と根拠

ORDレコード
ord-1be5f7fbe9ba40948c770f66502e1907
出典データセット
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08558006B2

反応ノート

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