反応 #321668

ord-d99fb27a6e594271a04dfbbb0dc4e232

反応方程式

[Cl][Mg][CH2]c1ccccc1
benzylmagnesium chloride
O=C1Nc2ccc(Cl)cc2C1=O
5-chloroisatin
[Cl-].[NH4+]
ammonium chloride
O=C1Nc2ccc(Cl)cc2C1(O)Cc1ccccc1
expected product
O=C1Nc2ccc(Cl)cc2C1(O)Cc1ccccc1
3-Benzyl-5-chloro-1,3-dihydro-3-hydroxyindol-2-one

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度is cooled to +4° C.
  2. 2
    濃縮the solvents are concentrated under vacuum
  3. 3
    抽出The aqueous phase is extracted with AcOEt
  4. 4
    洗浄the organic phase is washed with a saturated solution of NaCl and with water
  5. 5
    乾燥dried over sodium sulfate
  6. 6
    その他the solvent is evaporated off under vacuum

実験手順

A suspension of 10 g of 5-chloroisatin in 150 ml of THF is cooled to +4° C., 220 ml of a 1M solution of benzylmagnesium chloride in ether are added dropwise and the mixture is stirred for 3 hours at RT. 500 ml of a saturated solution of ammonium chloride are added and the solvents are concentrated under vacuum. The aqueous phase is extracted with AcOEt, the organic phase is washed with a saturated solution of NaCl and with water and dried over sodium sulfate and the solvent is evaporated off under vacuum to give 5.6 g of the expected product after crystallization from a THF/AcOEt mixture. M.p.=204°-205° C.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05594023uspto-grants-1997_01