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Hydrochloric Acid → 5-Nitro-indan-2-ylamine hydrochloride

HRID 1814773
Notes
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Reaction equation

HRID 1814773 reaction equation
[N+:1]([C:4]1[CH:5]=[C:6]2[C:10](=[CH:11][CH:12]=1)[CH2:9][CH:8]([NH:13]C(=O)C)[CH2:7]2)([O-:3])=[O:2].[ClH:17]>>[ClH:17].[NH2:13][CH:8]1[CH2:7][C:6]2[C:10](=[CH:11][CH:12]=[C:4]([N+:1]([O-:3])=[O:2])[CH:5]=2)[CH2:9]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 313Hydrochloric AcidHCID 14820512N-(5-nitro-indan-2-yl)-acetamide

Product 1

HCID 223193245-Nitro-indan-2-ylamine hydrochloride

Procedure

To N-(5-nitro-indan-2-yl)-acetamide (23.5 g, 107 mmol) is added 2N hydrochloric acid (500 mL). The mixture is heated to reflux for 24 h and then concentrated in vacuo. Methanol (100 mL) is added to the residue and the mixture is concentrated in vacuo. Toluene (100 mL) is added and the mixture is again concentrated. A solution of the residue in methanol (100 mL) is warmed, diethyl ether (500 mL) is added and the mixture is let stand overnight. The solid is collected by filtration and air dried to yield 2-amino-5-nitroindane hydrochloride as a white solid.

Workup

  1. temperatureThe mixture is heated
  2. temperatureto reflux for 24 h
  3. concentrationconcentrated in vacuo
addition
Methanol (100 mL) is added to the residue
  • concentrationthe mixture is concentrated in vacuo
  • additionToluene (100 mL) is added
  • concentrationthe mixture is again concentrated
  • temperatureA solution of the residue in methanol (100 mL) is warmed
  • additiondiethyl ether (500 mL) is added
  • filtrationThe solid is collected by filtration and air
  • customdried
  • Sources & evidence

    ORD record
    ord-5551f9a7e51f4eb58cad8f44d790f270
    Source dataset
    uspto-grants-2005_04
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US06878707B2

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes