反応 #2254180

ord-d632c73ed8c04d9480f4f695ecf513c4

反応方程式

CC(=O)[O-].[Na+]
Sodium acetate
Cl.NO
hydroxylamine hydrochloride
Cc1cc(C=O)sc1C(=O)NCC(F)(F)F
5-formyl-3-methyl-thiophene-2-carboxylic acid (2,2,2-trifluoro-ethyl)-amide
Cc1cc(C=NO)sc1C(=O)NCC(F)(F)F
5-(hydroxyimino-methyl)-3-methyl-thiophene-2-carboxylic acid (2,2,2-trifluoro-ethyl)-amide

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他the reaction is quenched with water
  2. 2
    抽出The reaction mixture is extracted three times with ethyl acetate
  3. 3
    乾燥The combined organic phases are dried over Na2SO4
  4. 4
    濃縮concentrated in vacuo

実験手順

Sodium acetate (90 mg) is added to a solution of hydroxylamine hydrochloride (60 mg) and 5-formyl-3-methyl-thiophene-2-carboxylic acid (2,2,2-trifluoro-ethyl)-amide (190 mg) in THF (5 ml), water (1 ml) and DMSO (1 ml). After 3 hours at room temperature, the reaction is quenched with water. The reaction mixture is extracted three times with ethyl acetate. The combined organic phases are dried over Na2SO4 and concentrated in vacuo to yield 5-(hydroxyimino-methyl)-3-methyl-thiophene-2-carboxylic acid (2,2,2-trifluoro-ethyl)-amide. The crude product obtained (206 mg, yellowish oil) is used without further purification. MS (HPLC/MS): 267 (MH+). Retention time: 2.56 min and 2.64 min (two diastereoisomers).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US09044389B2uspto-grants-2015_06