Borane;tetrahydrofuran → HCID 24826940、化合物

HRID 63831ノート

反応式

HRID 63831 の反応式
[Cl:1][CH2:2][CH2:3][NH:4][C:5](=O)[C:6]([F:9])([F:8])[F:7].B.C1COCC1>O1CCCC1>[Cl:1][CH2:2][CH2:3][NH:4][CH2:5][C:6]([F:9])([F:8])[F:7]

参加物

4

実験手順

Into a 500-mL round-bottom flask, was placed a solution of N-(2-chloroethyl)-2,2,2-trifluoroacetamide (17.6 g, 100.26 mmol, 1.00 equiv) in tetrahydrofuran (50 mL). This was followed by the addition of BH3.THF (200 mL) dropwise with stirring. The resulting solution was heated to reflux overnight in an oil bath. The resulting mixture was concentrated under vacuum. The resulting solution was diluted with 200 mL of H2O. The resulting solution was extracted with 3×100 mL of ethyl acetate and the organic layers combined and dried over anhydrous sodium sulfate and concentrated under vacuum. This resulted in 15 g (crude) of (2-chloroethyl)(2,2,2-trifluoroethyl)amine as yellow oil. (ES, m/z): 163 [M+H]+

後処理

  1. customInto a 500-mL round-bottom flask, was placed
  2. temperatureThe resulting solution was heated
  3. temperatureto reflux overnight in an oil bath
  4. concentrationThe resulting mixture was concentrated under vacuum
  5. additionThe resulting solution was diluted with 200 mL of H2O
  6. extractionThe resulting solution was extracted with 3×100 mL of ethyl acetate
  7. dry with materialdried over anhydrous sodium sulfate
  8. concentrationconcentrated under vacuum
  9. customThis resulted in 15 g (crude) of (2-chloroethyl)(2,2,2-trifluoroethyl)amine as yellow oil

出典と根拠

ORDレコード
ord-1b6e89da98cf4847bca12c3681be0ae7
出典データセット
uspto-grants-2016_09
特許番号
US09447084B2

反応ノート

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