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Chemical Structure| 112734-23-3 Chemical Structure| 112734-23-3

Structure of 112734-23-3

Chemical Structure| 112734-23-3

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Product Details of [ 112734-23-3 ]

CAS No. :112734-23-3
Formula : C8H3Cl2NO3
M.W : 232.02
SMILES Code : O=C1OC(NC2=CC(Cl)=CC(Cl)=C21)=O
MDL No. :MFCD14706088

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Application In Synthesis of [ 112734-23-3 ]

* 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 [ 112734-23-3 ]

[ 112734-23-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 18711-15-4 ]
  • [ 112734-23-3 ]
YieldReaction ConditionsOperation in experiment
72% With acetic anhydride; In acetic acid; a. 5,7-Dichloro-2H-3,1-benzoxazine-2,4(1H)-dione To a stirred solution of <strong>[18711-15-4]4,6-dichloro-1H-indole-2,3-dione</strong> (5.00 g, 23.2 mM) in acetic acid (21 mL) and acetic anhydride (21 mL) at 80 C. was added in small portions chromium trioxide (4.12 g, 41.3 mM). The temperature of the reaction mixture was maintained between 80-90 C. during the addition of the chromium trioxide. After the addition was complete, the reaction mixture was diluted with water (100 mL) and then filtered to separate the precipitated solids. The solids were washed thoroughly with water and then dried to obtain the title compound as a yellow solid (4.13 g, 72%); MS(CI): 232 (M+H).
In acetic acid; PREPARATION 10 To a suspension of <strong>[18711-15-4]4,6-dichloroindolin-2,3-dione</strong> (5.95 g) in acetic acid (95 ml) was added chromium trioxide (16 g) over a period of 15 minutes at 60 C. with stirring and the mixture was stirred at 70-75 C. for 1 hour. After cooling, the reaction mixture was poured into water (360 ml) and the resulting precipitates were collected by filtration. The filtrate was extracted with ethyl acetate. The extract was washed with water and dried. Removal of the solvent gave a residue, which was combined with the precipitates. Recrystallization from isopropyl ether gave 5,7-dichloro-2H-3,1-benzoxazine-2,4(1H)-dione (2.85 g). mp: 267-268 C. IR (Nujol): 3225, 3200, 3100, 3075, 1790, 1775, 1705, 1610, 1585 cm-1. NMR (DMSO-d6, delta): 7.09 (1H, d, J=1.2 Hz), 7.48 (1H, d, J=1.2 Hz).
 

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