HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

Sulfuric Acid → 7-nitro-2,3-dihydro-1H-indole-2,3-dione

HRID 1470575
Notes
Print preview

Reaction equation

HRID 1470575 reaction equation
ON=[CH:3][C:4]([NH:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[N+:13]([O-:15])=[O:14])=[O:5].S(=O)(=O)(O)[OH:17]>>[N+:13]([C:8]1[CH:9]=[CH:10][CH:11]=[C:12]2[C:7]=1[NH:6][C:4](=[O:5])[C:3]2=[O:17])([O-:15])=[O:14]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 1118Sulfuric AcidHCID 6785498HCID 6785498, compound

Product 1

HCID 38583087-nitro-2,3-dihydro-1H-indole-2,3-dione

Procedure

2-Hydroxyimino-N-(2-nitro-phenyl)-acetamide (15 g, 72 mmol) was carefully added in small portions to a stirred solution of preheated (90° C.) conc. sulphuric acid (45 mL) over a period of 30 min and the resulting mixture was stirred for another 2 h at the same temperature. It was then cooled to room temperature, poured into crushed ice, the precipitated products was collected by filtrations. The collected precipitated products were washed with water and dried in a vacuum oven to get a brick red colour powder.

Workup

  1. customof 30 min
  2. additionpoured
  3. custominto crushed ice
  4. filtrationthe precipitated products was collected by filtrations
custom
The collected precipitated products
  • washwere washed with water
  • customdried in a vacuum oven
  • customto get a brick red colour powder
  • Sources & evidence

    ORD record
    ord-3fd57298327d4cbea43d24359a686519
    Source dataset
    uspto-grants-2015_04
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US09006454B2

    Reaction notes

    Loading…

    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes