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Methanol → Methyl 1-(difluoromethyl)-1H-pyrazole-3-carboxylate

HRID 403263
ノート
印刷プレビュー

反応式

HRID 403263 の反応式
[F:1][CH:2]([F:11])[N:3]1[CH:7]=[CH:6][C:5]([C:8]([OH:10])=[O:9])=[N:4]1.S(=O)(=O)(O)O.[CH3:17]O>>[CH3:17][O:9][C:8]([C:5]1[CH:6]=[CH:7][N:3]([CH:2]([F:1])[F:11])[N:4]=1)=[O:10]
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 887MethanolHCID 1118Sulfuric AcidHCID 31541781-(Difluoromethyl)-1H-pyrazole-3-carboxylic acid

生成物 1

HCID 57497167Methyl 1-(difluoromethyl)-1H-pyrazole-3-carboxylate

反応条件

温度
23 °C

実験手順

A solution of 1-difluoromethyl-1H-pyrazole-3-carboxylic acid (CAS [925179-02-8]) (500 mg, 3.1 mmole) in methanol (18 ml) was cooled to 0° C. and treated with sulfuric acid (98%, 0.2 ml, 3.1 mmol). The mixture was heated to reflux for 2 hours, cooled to 23° C. and concentrated at reduced pressure. The residue was partitioned between AcOEt and water, the organic layer was washed with water until the water phase showed a neutral pH, dried and evaporated to give the title compound (535 mg) as a colorless liquid which was used without further purification. MS: m/z=177.1 [M+H]+.

後処理

  1. temperatureThe mixture was heated
  2. temperatureto reflux for 2 hours
  3. concentrationconcentrated at reduced pressure
  4. customThe residue was partitioned between AcOEt and water
  5. washthe organic layer was washed with water until the water phase
  6. customdried
  7. customevaporated

出典と根拠

ORDレコード
ord-df414fa38c48451dba5d59009f63c3ca
出典データセット
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08748418B2

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート