反応 #58586

ord-8a9d54343363425284812cb537300fa9

反応方程式

O.[Na+].[OH-]
NaOH H2O
N#Cc1ccccc1N
anthranilonitrile
[Br][Mg][CH]1CCCC1
cyclopentylmagnesium bromide
Cl
HCl
Nc1ccccc1C(=O)C1CCCC1
crude product
収率 93.6%
Nc1ccccc1C(=O)C1CCCC1
2-aminophenyl cyclopentylmethanone
収率 93.6%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.STIRRINGThe mixture was stirred at room temperature for 1 hour
  2. 2
    抽出to extract the aqueous layer
  3. 3
    乾燥The combined organic layers were dried over Na2SO4
  4. 4
    その他The solvent was removed

実験手順

To a solution of anthranilonitrile (15.0 g) in diethyl ether (600 mL) was added a solution of 2.0 M cyclopentylmagnesium bromide in diethyl ether (159 mL) at 0° C. under nitrogen. The mixture was stirred at room temperature overnight (20 hours). 500 ml of 5 N HCl in H2O was added very slowly at 0° C. The mixture was stirred at room temperature for 1 hour. The aqueous layer was neutralized with 50% NaOH/H2O to pH=12. 2×500 mL of ethyl acetate was used to extract the aqueous layer. The combined organic layers were dried over Na2SO4. The solvent was removed to give the crude product 22.5 g (93.6% yield). H1NMR (CDCl3): δ6.62-7.82 (m, 4H), 3.64-3.78 (m, 1H), 1.50-1.96 (m, 8H).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07423033B2uspto-grants-2008_09