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

HRID 1531267
Notes
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Reaction equation

HRID 1531267 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 a white solid.

Workup

  1. temperatureThe mixture is heated
  2. temperatureto reflux for 24 h
  3. concentrationconcentrated in vacuo
  4. 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
  • customto yield a white solid
  • Sources & evidence

    ORD record
    ord-cc2838fb3002459ca7190ddfec0b9b71
    Source dataset
    uspto-grants-2001_03
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US06197798B1

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes