Aniline → N-(2-Methylbut-3-yn-2-yl)aniline

HRID 351581Notes

Reaction equation

HRID 351581 reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(N(CC)CC)C.Cl[C:16]([CH3:20])([CH3:19])[C:17]#[CH:18]>CCOCC.O.[Cu]Cl.[Cu]>[CH3:19][C:16]([NH:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1)([CH3:20])[C:17]#[CH:18]

Participants

8

Conditions

Temperature
15 °C

Procedure

A mixture of aniline (21.8 g, 234 mmol) and triethylamine (26.6 g, 263.3 mmol) in 100 mL ether, 25 mL water, 0.2 g copper(I) chloride and 0.2 g copper bronze was prepared under nitrogen in a three-neck flask equipped with mechanical stirrer. 3-Chloro-3-methyl-1-butyne (20 g, 195 mmol) in ether (25 mL) was slowly added with stirring while maintaining an inside temperature at 10-20° C. After stirring for an additional 2 hours at room temperature, the mixture was poured into a mixture of 200 mL ether and 100 mL water. The ethereal layer was washed with cold water, dried for 15 minutes over anhydrous potassium carbonate and filtered, redried with potassium hydroxide pellets overnight. The solution was filtered and concentrated under reduced pressure.

Workup

  1. customwas prepared under nitrogen in a three-neck flask
  2. customequipped with mechanical stirrer
  3. stirringAfter stirring for an additional 2 hours at room temperature
  4. washThe ethereal layer was washed with cold water
  5. dry with materialdried for 15 minutes over anhydrous potassium carbonate
  6. filtrationfiltered
  7. dry with materialredried with potassium hydroxide pellets overnight
  8. filtrationThe solution was filtered
  9. concentrationconcentrated under reduced pressure

Sources & evidence

ORD record
ord-d60c506a86a04617a3d79a0c8d54335a
Source dataset
uspto-grants-2004_06
Patent number
US06743785B2

Reaction notes

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