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Acetic Acid → 5,7-dichloro-2,4-dihydro-1H-3,1-benzoxazine-2,4-dione

HRID 3103
Notes
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Reaction equation

HRID 3103 reaction equation
[Cl:1][C:2]1[CH:10]=[C:9]([Cl:11])[CH:8]=[C:7]2[C:3]=1[C:4](=[O:13])[C:5](=[O:12])[NH:6]2.C(O)(=[O:16])C>C(OC(=O)C)(=O)C.O.[O-2].[O-2].[O-2].[Cr+6]>[Cl:1][C:2]1[C:3]2[C:4](=[O:13])[O:12][C:5](=[O:16])[NH:6][C:7]=2[CH:8]=[C:9]([Cl:11])[CH:10]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 2

HCID 176Acetic AcidHCID 2519084,6-Dichloroisatin

Product 1

HCID 123632155,7-dichloro-2,4-dihydro-1H-3,1-benzoxazine-2,4-dioneYield 72%

Reagents, catalysts & solvents 3

HCID 10219390chromium (VI) trioxideCatalyst2×HCID 962WaterSolvent
HCID 7918
Acetic Anhydride
Solvent

Procedure

To a stirred solution of 4,6-dichloro-1H-indole-2,3-dione (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).

Workup

  1. additionAfter the addition
  2. filtrationfiltered
  3. customto separate the precipitated solids
  4. washThe solids were washed thoroughly with water
  5. customdried

Sources & evidence

ORD record
ord-62f911c33ec34c2dbe633593e1d5ee82
Source dataset
uspto-grants-1998_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05733910

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes