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Chemical Structure| 352030-17-2 Chemical Structure| 352030-17-2

Structure of 352030-17-2

Chemical Structure| 352030-17-2

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Product Details of [ 352030-17-2 ]

CAS No. :352030-17-2
Formula : C12H16ClNO2
M.W : 241.71
SMILES Code : O=C(OC(C)(C)C)NC1=CC=C(Cl)C(C)=C1
MDL No. :N/A

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Application In Synthesis of [ 352030-17-2 ]

* 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 [ 352030-17-2 ]

[ 352030-17-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 24424-99-5 ]
  • [ 7149-75-9 ]
  • [ 352030-17-2 ]
YieldReaction ConditionsOperation in experiment
36% In dichloromethane; at 0 - 20℃; for 20h;Inert atmosphere; 4-Chloro-3-methylaniline (1 .00 g, 7.06 mmol) was dissolved in 15 ml of DCM and cooled to 0°C under N2. Boc anhydride (1.70 g, 7.77 mmol) was then added portion wise to the reaction which was allowed to warm to 20°C and stirred for 20 h. The organic layer was then washed with water (15 ml), brine (15 ml), dried with Na2S04, filtered and concentrated in vacuo. The crude residue was then purified by column chromatography (100percent CyHex to 10percent EtOAc/CyHex) to obtain WIN-330-031-01 as white crystals (608 mg, 36percent). 1 H NMR (CDCI3): delta 7.30 (d, J 2.4 Hz, 1 H), 7.21 (d, J 8.8 Hz, 1 H), 7.05 - 7.1 1 (m, 1 H), 6.48 (br s, 1 H), 2.33 (s, 3H), 1.51 (s, 9H).
In 1,4-dioxane; at 20℃; for 24h; A mixture of 10 g of <strong>[7149-75-9]4-chloro-3-methylaniline</strong> and 15.26 g of di-tert-butyl dicarbonate in 50 ml of dioxane is stirred at RT for 24 hours. The reaction mixture is concentrated under vacuum and the residue is chromatographed on silica gel, eluting with a DCM/hexane mixture gradient from (50/50; v/v) to (70/30; v/v). 5.6 g of the expected product are obtained, and are used without further purification.
 

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