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Chemical Structure| 38405-48-0 Chemical Structure| 38405-48-0

Structure of 38405-48-0

Chemical Structure| 38405-48-0

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Product Details of [ 38405-48-0 ]

CAS No. :38405-48-0
Formula : C8H9NO2S
M.W : 183.23
SMILES Code : SC1=CC(C)=C([N+]([O-])=O)C=C1C
MDL No. :MFCD28108142

Safety of [ 38405-48-0 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H301+H311+H331-H315-H319
Precautionary Statements:P501-P261-P270-P271-P264-P280-P337+P313-P305+P351+P338-P361+P364-P332+P313-P301+P310+P330-P302+P352+P312-P304+P340+P311-P403+P233-P405
Class:6.1
UN#:2810
Packing Group:

Application In Synthesis of [ 38405-48-0 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 38405-48-0 ]

[ 38405-48-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 38405-48-0 ]
  • [ 262587-05-3 ]
  • [ 1361046-19-6 ]
YieldReaction ConditionsOperation in experiment
With sodium hydride;copper; copper(l) chloride; In N,N-dimethyl-formamide; at 0 - 150℃; for 1h; EXAMPLE 1; Preparation of 2-nitro-5- (3-difluoromethoxyphenylthio) - p-xylene [nitroderivative of formula (III) ]; 4.36 g (0.109 moles) of sodium hydride are sus¬ pended in 80 ml of N, N-dimethylformamide at 0C. 20 g of 4-nitro-2 , 5-dimethylthiophenol (0.109 moles) dis¬ solved in 67 ml of N, N-dimethylformamide are added dropwise under stirring. 24.4 g of l-bromo-3- (difluoromethoxy) benzene (0.109 moles) dissolved in 20 ml of N, N-dimethylformamide are then added dropwise; catalytic Cu and CuCl are subsequently added and the reaction temperature is brought to 150 C for 1 h.After GC control, the reaction mixture is cooled to room temperature, filtered on a celite bed, diluted with water and extracted with ethyl acetate. The or¬ ganic phase is anhydrified with sodium sulfate, and then filtered and evaporated.The product thus obtained is purified on silica gel eluting with hexane/ethyl acetate 9:1. 30 g of the desired product are obtained. GC-MS : M+ = 325
30 g With copper; sodium hydride; copper(l) chloride; In N,N-dimethyl-formamide; mineral oil; at 0 - 150℃; for 1h; EXAMPLE 1 Preparation of 2-nitro-5-(3-difluoromethoxyphenylthio)-p-xylene [nitroderivative of formula (III)] 4.36 g (0.109 moles) of sodium hydride are suspended in 80 ml of N,N-dimethylformamide at 0 C. 20 g of 4-nitro-2,5-dimethylthiophenol (0.109 moles) dissolved in 67 ml of N,N-dimethylformamide are added dropwise under stirring. 24.4 g of <strong>[262587-05-3]1-bromo-3-(difluoromethoxy)benzene</strong> (0.109 moles) dissolved in 20 ml of N,N-dimethylformamide are then added dropwise; catalytic Cu and CuCl are subsequently added and the reaction temperature is brought to 150 C. for 1 h. After GC control, the reaction mixture is cooled to room temperature, filtered on a celite bed, diluted with water and extracted with ethyl acetate. The organic phase is anhydrified with sodium sulfate, and then filtered and evaporated. The product thus obtained is purified on silica gel eluting with hexane/ethyl acetate 9:1. 30 g of the desired product are obtained. GC-MS: M+=325
 

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