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Chemical Structure| 24805-54-7 Chemical Structure| 24805-54-7

Structure of 24805-54-7

Chemical Structure| 24805-54-7

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Product Details of [ 24805-54-7 ]

CAS No. :24805-54-7
Formula : C10H11NO4
M.W : 209.20
SMILES Code : O=C(OC)C1=CC=C(C)C([N+]([O-])=O)=C1C
MDL No. :MFCD23703478

Safety of [ 24805-54-7 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P264-P270-P301+P312-P330

Application In Synthesis of [ 24805-54-7 ]

* 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 [ 24805-54-7 ]

[ 24805-54-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 67-56-1 ]
  • [ 201230-82-2 ]
  • [ 56404-21-8 ]
  • [ 24805-54-7 ]
YieldReaction ConditionsOperation in experiment
98% With palladium diacetate; triethylamine; 1,4-di(diphenylphosphino)-butane; In acetonitrile; at 100℃; under 4137.41 Torr; for 2.0h;Autoclave; Sealed tube; Scheme 4, Step B: To a 2 L Parr autoclave with mechanical stirring is added <strong>[56404-21-8]1-iodo-2,4-dimethyl-3-nitro-benzene</strong> (70 g, 252.7 mmol), Pd(OAc)2 (2.8 g, 12.6 mmol),1 ,4-bis( diphenylphosphino )butane ( 6.5 g, 15.2 mmol), acetonitrile ( 462 mL ),triethylamine (88.2 mL), and methanol (280 mL). The Parr autoclave is sealed, purgedand pressurized with CO to 551.6 kPa (80 psig). The mixture is heated to 100C for 2hours. The mixture is cooled to ambient temperature and then vented. The mixture isthen concentrated to dryness under reduced pressure. Ethyl acetate (300 mL) and water(300 mL) are added. The layers are separated and the aqueous layer discarded. The organic layer is dried over MgS04, filtered, and concentrated to dryness to afford the title20compound as a red oil which crystallizes upon standing (52 g, 98 %). 1 H NMR (300.13MHz, CDCl3): o 7.89 (d, J= 8.2 Hz, 1H), 7.19 (d, J= 8.2 Hz, 1H), 3.91 (s, 3H), 2.49 (s,3H), 2.33 (s, 3H).
98% With palladium diacetate; triethylamine; 1,4-di(diphenylphosphino)-butane; In acetonitrile; at 100℃; under 4137.41 Torr; for 2.0h;Autoclave; To a 2 L Parr autoclave with mechanical stirring is added 1- iodo-2,4-dimethyl-3-nitro-benzene (70 g, 252.7 mmol), Pd(OAc)2 (2.8 g, 12.6 mmol), l,4-bis(diphenylphosphino)butane (6.5 g, 15.2 mmol), acetonitrile (462 mL), triethylamine (88.2 mL), and MeOH (280 mL). The Parr autoclave is sealed, purged, and pressurized with CO to 551.6 kPa (80 psig). The mixture is heated to 100 C for 2 hours. The mixture is cooled to ambient temperature and then vented. The mixture is then concentrated to dryness under reduced pressure. EtOAc (300 mL) and water (300 mL) are added. The layers are separated, and the aqueous layer discarded. The organic layer is dried over MgS04, filtered, and concentrated to dryness to afford methyl 2,4-dimethyl- 3-nitro-benzoate as a red oil that crystallizes upon standing (52 g, 98 %). 1H NMR (300.13 MHz, CDC13): delta 7.89 (d, J= 8.2 Hz, 1H), 7.19 (d, J= 8.2 Hz, 1H), 3.91 (s, 3H), 2.49 (s, 3H), 2.33 (s, 3H).
 

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