Réaction #48313

ord-84f384e1b4ca4b4897235a5af4920794

Équation de réaction

O
water
Nc1ccc(Br)cc1
4-bromobenzenamine
O
water
C#CC(C)(C)Cl
3-chloro-3-methylbut-1-yne
C#CC(C)(C)Nc1ccc(Br)cc1
product
C#CC(C)(C)Nc1ccc(Br)cc1
4-bromo-N-(2-methylbut-3-yn-2-yl)benzenamine

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autrethe reaction mixture was transferred to a seperatory funnel
  2. 2
    LavageThe aqueous layer was washed 3× with EtOAc
  3. 3
    Séchagedried with MgSO4
  4. 4
    Filtrationfiltered
  5. 5
    Concentrationconcentrated
  6. 6
    AutreThe crude oil was purified with by MPLC (100% DCM to 10% (91/10/1 DCM:MeOH:NH4OH))

Mode opératoire

To a solution of 4-bromobenzenamine (4.0 g, 23 mmol), TEA (4.3 ml, 31 mmol), 2.0 ml of water, copper (0.058 g, 0.91 mmol) and copper(I) chloride (0.058 g, 0.59 mmol) in diethyl ether (9.8 ml, 20 mmol) was added 3-chloro-3-methylbut-1-yne (2.0 g, 20 mmol), dropwise. After stirring overnight, the reaction mixture was transferred to a seperatory funnel containing water and diethyl ether. The aqueous layer was washed 3× with EtOAc. The organic layers were combined, dried with MgSO4, filtered and concentrated. The crude oil was purified with by MPLC (100% DCM to 10% (91/10/1 DCM:MeOH:NH4OH)) to provide the product as an oil. MS m/z: 240 (M+2).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07745484B2uspto-grants-2010_06