Water → n,n-Bis(2,2,2-trifluoroethyl)-3-methyl-4-nitroaniline

HRID 538955

反応式

HRID 538955 の反応式
[CH3:1][C:2]1[CH:3]=[C:4]([CH:6]=[CH:7][C:8]=1[N+:9]([O-:11])=[O:10])[NH2:5].[BH4-].[Na+].O.[F:15][C:16]([F:21])([F:20])[C:17](O)=O>>[F:15][C:16]([F:21])([F:20])[CH2:17][N:5]([CH2:17][C:16]([F:21])([F:20])[F:15])[C:4]1[CH:6]=[CH:7][C:8]([N+:9]([O-:11])=[O:10])=[C:2]([CH3:1])[CH:3]=1

参加物

5

反応物 4

HCID 962WaterHCID 6422Trifluoroacetic acidHCID 118984-Nitro-m-toluidineHCID 4311764Sodium borohydride

生成物 1

HCID 11243980n,n-Bis(2,2,2-trifluoroethyl)-3-methyl-4-nitroaniline収率 82%

反応条件

温度
60 °C

実験手順

3-Methyl-4-nitroaniline 3.9 g (25 mmol) was dissolved in 100 mL of trifluoroacetic acid with stirring under N2 at 60° C. Next, sodium borohydride pellets (14 g, 15 eq.) were added portionwise. Ten minutes after the addition of the pellets, the reaction was heated to 90° C. After 12 h at 90° C., the reaction was cooled, added slowly to water, and then filtered. The resulting solid filtrate was washed first with water and then with hexanes and was then dried. This procedure resulted in 6.6 g (82% yield) of a light yellow powder. Data for compound 101: 1H-NMR (CDCl3, 500 MHz) 8.10 (d, 1H, J=9.3 Hz), 6.78 (dd, 1H, J=9.3 and 2.9 Hz), 6.72 (d, 1H, J=2.9 Hz), 4.13 (q, 4H, J=8.4 Hz), 2.66 (s, 3H).

後処理

  1. additionTen minutes after the addition of the pellets
  2. temperaturethe reaction was heated to 90° C
  3. temperaturethe reaction was cooled
  4. filtrationfiltered
  5. washThe resulting solid filtrate was washed first with water
  6. dry with materialwith hexanes and was then dried

出典と根拠

ORDレコード
ord-0c138a7e890544fab3f32743ae6f0f52
出典データセット
uspto-grants-2014_10
特許番号
US08865918B2

関連ノート

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