تفاعل #58664

ord-7bfa1ec39dbd48a2aa8e06da725808db

معادلة التفاعل

CN(C)c1ccccc1-c1ccccc1P(C1CCCCC1)C1CCCCC1
2-dicyclohexylphospino-2′-(N,N-dimethylamino) biphenyl
Cn1ccc2c(Cl)cccc21
4-chloro-1-methylindole
C=C(C)OC(C)=O
isopropenyl acetate
CCC[CH2][Sn+]([CH2]CCC)[CH2]CCC.C[O-]
tributyltin methoxide
CC(=O)Cc1cccc2c1ccn2C
title compound
CC(=O)Cc1cccc2c1ccn2C
1-(1-Methyl-1H-indol-4-yl)acetone

المذيبات

ظروف التفاعل

درجة الحرارة
100°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONwere added
  2. 2
    درجة الحرارةheating
  3. 3
    درجة الحرارةAfter 2 h the solution was cooled
  4. 4
    ترشيحfiltered through a pad of CELITE diatomaceous earth
  5. 5
    تركيزthe filtrate was concentrated to ca. 5 mL
  6. 6
    أخرىThis solution was purified on a silica column

الإجراء التجريبي

To a solution of 0.852 g (5.14 mmol) of 4-chloro-1-methylindole in 15 mL dry toluene, 0.85 mL (7.73 mmol) isopropenyl acetate and 2.3 ml (8 mmol) tributyltin methoxide were added. The solution was heated to 100° C. After 15 min, 0.24 g (0.61 mmol) 2-dicyclohexylphospino-2′-(N,N-dimethylamino) biphenyl and 0.14 g (0.153 mmol) tris (dibenzylidineacetone)dipalladium were added and heating was continued. After 2 h the solution was cooled, filtered through a pad of CELITE diatomaceous earth and the filtrate was concentrated to ca. 5 mL. This solution was purified on a silica column using a gradient of 5-20% EtOAc/hexane to obtain the title compound. 1H NMR: (500 MHz, CDCl3): δ 2.14 (s, 3H), 3.84 (s, 3H), 3.97 (s, 2H), 6.51 (d, 1H), 7-7.3 (m, 4H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07423067B2uspto-grants-2008_09