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Hydrochloric Acid → HCID 86752147, compound

HRID 863526
Notes
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Reaction equation

HRID 863526 reaction equation
[N:1]#[N:2].[CH3:3][CH:4]1[C:12]2[C:7](=[C:8]([N+:18]([O-:20])=[O:19])[C:9]([NH:14]C(=O)C)=[C:10]([Br:13])[CH:11]=2)[CH2:6][CH:5]1[NH:21]C(=O)C.[ClH:25]>C(O)(=O)C>[N:1]#[N:2].[ClH:25].[CH3:3][CH:4]1[C:12]2[C:7](=[C:8]([N+:18]([O-:20])=[O:19])[C:9]([NH2:14])=[C:10]([Br:13])[CH:11]=2)[CH2:6][CH:5]1[NH2:21]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 313Hydrochloric AcidHCID 86752145HCID 86752145, compound

Product 1

HCID 86752147HCID 86752147, compound

Reagents, catalysts & solvents 1

HCID 176Acetic AcidSolvent

Conditions

Temperature
100 °C

Procedure

A mixture of N2 -methyl-2,5-diacetamido-6-bromo-4-nitroindane (22.5 g, 61 mmol) in 3N HCl (150 mL) and acetic acid (50 mL) was heated at 100° C. for 24 h. The mixture was cooled in an ice bath and the orange precipitate was collected by filtration and dried (17.2 g).

On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Workup

  1. temperatureThe mixture was cooled in an ice bath
  2. filtrationthe orange precipitate was collected by filtration
  3. customdried (17.2 g)

Sources & evidence

ORD record
ord-2d83098898034772877b76ddee85339f
Source dataset
uspto-grants-1998_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05721234

Reaction notes

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