反応 #474880

ord-cb1677c95590495b8c0089f126a3a9b6

反応方程式

O=C(OO)c1cccc(Cl)c1
3-chloroperbenzoic acid
CCN(CC)CC
triethylamine
O=C(Cl)Oc1ccccc1
phenyl chloroformate
CSc1cccc(N)c1
1-Amino-3-methylthiobenzene
O=S([O-])([O-])=S.[Na+].[Na+]
sodium thiosulfate
CS(=O)(=O)c1cccc(NC(=O)Oc2ccccc2)c1
title compound
収率 87.4%
CS(=O)(=O)c1cccc(NC(=O)Oc2ccccc2)c1
Phenyl-3-methylsulfonylphenylcarbamate
収率 87.4%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    洗浄the organic layer was washed with saturated saline
  2. 2
    乾燥dried over anhydrous sodium sulfate
  3. 3
    workup.DISTILLATIONAfter distilling off the solvent
  4. 4
    その他drying under reduced pressure
  5. 5
    workup.DISSOLUTIONthe residue was dissolved in dichloromethane (50 ml)
  6. 6
    温度while cooling in an ice water bath
  7. 7
    ろ過the insoluble portion was filtered off
  8. 8
    抽出extraction with ethyl acetate
  9. 9
    洗浄by washing with an aqueous saturated solution of sodium carbonate
  10. 10
    乾燥drying over anhydrous sodium sulfate
  11. 11
    workup.DISTILLATIONThe solvent was distilled off
  12. 12
    その他the residue was purified by silica gel column chromatography (ethyl acetate-hexane=1:1)

実験手順

1-Amino-3-methylthiobenzene (1.27 ml, 10 mmol) was dissolved in tetrahydrofuran (10 ml), and then triethylamine (1.46 ml, 10.5 mmol) and phenyl chloroformate (1.32 ml, 10.5 mmol) were added dropwise in that order at room temperature under a nitrogen atmosphere and the mixture was stirred overnight. The reaction solution was distributed between ethyl acetate and water, and the organic layer was washed with saturated saline and dried over anhydrous sodium sulfate. After distilling off the solvent and drying under reduced pressure, the residue was dissolved in dichloromethane (50 ml), and 3-chloroperbenzoic acid (4.93 g, 20 mmol) was gradually added while cooling in an ice water bath. An aqueous saturated solution of sodium thiosulfate was added to the reaction solution, and then the insoluble portion was filtered off, and extraction with ethyl acetate was followed by washing with an aqueous saturated solution of sodium carbonate and drying over anhydrous sodium sulfate. The solvent was distilled off, and the residue was purified by silica gel column chromatography (ethyl acetate-hexane=1:1) to obtain the title compound (2.545 g, 8.74 mmol, 87.4%) as white crystals.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08372981B2uspto-grants-2013_02