Dicyclohexylcarbodiimide → 2-Propenamide, N-methoxy-N-methyl-2-(trifluoromethyl)-

HRID 1948158

反応式

HRID 1948158 の反応式
Cl.[CH3:2][NH:3][O:4][CH3:5].C(N(CC)C(C)C)(C)C.[F:15][C:16]([F:23])([F:22])[C:17](=[CH2:21])[C:18](O)=[O:19].C1(N=C=NC2CCCCC2)CCCCC1>C(Cl)Cl>[CH3:5][O:4][N:3]([CH3:2])[C:18](=[O:19])[C:17]([C:16]([F:23])([F:22])[F:15])=[CH2:21]

参加物

6

反応条件

温度
0 °C

実験手順

16.6 g (167 mmol) of N,O-dimethylhydroxylamine hydrochloride were suspended in 900 ml of CH2Cl2 and 29.1 ml (167 mmol) of N,N-diisopropylethylamine added dropwise at 0° C. The resulting solution was added dropwise to a solution of 20.0 g (143 mmol) of 2-(trifluoromethyl)propenoic acid in 500 ml of CH2Cl2 at −40° C. Afterwards, 34.5 g (167 mmol) of N,N′-dicyclohexylcarbodiimide were added and the mixture stirred at 0° C. for 16 h. The resulting suspension was then filtrated and the filtrate carefully evaporated (the desired product is volatile!). Afterwards, 100 ml of n-pentane were added and the suspension stirred for 30 minutes at ambient temperature. The precipitate was removed by filtration, the filtrate was carefully evaporated. Chromatography on silica gel using ethyl acetate/n-pentane 1:4 yielded 22.8 g of the desired product. Rt=0.56 min (Method P).

後処理

  1. filtrationThe resulting suspension was then filtrated
  2. customthe filtrate carefully evaporated (the desired product
  3. additionAfterwards, 100 ml of n-pentane were added
  4. stirringthe suspension stirred for 30 minutes at ambient temperature
  5. customThe precipitate was removed by filtration
  6. customthe filtrate was carefully evaporated

出典と根拠

ORDレコード
ord-c388f139220f4d8a8bcd445f56f9cb9b
出典データセット
uspto-grants-2013_03
特許番号
US08399482B2

関連ノート

読み込み中…