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Ethanol → HCID 86602485, compound

HRID 1446552
Notes
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Reaction equation

HRID 1446552 reaction equation
C(O)C.[N:4]1([C:10]2[CH:11]=[C:12]3[C:16](=[CH:17][CH:18]=2)[C:15](=O)[CH2:14][CH2:13]3)[CH2:9][CH2:8][O:7][CH2:6][CH2:5]1.[Cl-].[OH:21][NH3+:22].C(N(CC)CC)C>C(OCC)(=O)C.O>[N:4]1([C:10]2[CH:11]=[C:12]3[C:16](=[CH:17][CH:18]=2)[C:15](=[N:22][OH:21])[CH2:14][CH2:13]3)[CH2:9][CH2:8][O:7][CH2:6][CH2:5]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 4

HCID 702EthanolHCID 8471TriethylamineHCID 21645Hydroxylamine HClHCID 461728755-(Morpholin-4-yl)-2,3-dihydro-1H-inden-1-one

Product 1

HCID 86602485HCID 86602485, compoundYield 96.9%

Reagents, catalysts & solvents 2

HCID 962
Water
Solvent
HCID 8857Ethyl AcetateSolvent

Procedure

An ethanol (5.0 mL) solution of 5-morpholin-4-yl-indan-1-one(2.20 g), hydroxyl ammonium chloride (1.05 g) and the triethylamine (4.22 mL) was refluxed for 3 hours. Water and ethyl acetate were added to the reaction solution, and the organic layer was partitioned. The obtained organic layer was washed with a saturated sodium chloride solution, and 2.28 g of the title compound was obtained by condensing under reduce pressure after drying over anhydrous magnesium sulfate. The physical properties of the compound are as follows.

Workup

  1. customthe organic layer was partitioned
  2. washThe obtained organic layer was washed with a saturated sodium chloride solution

Sources & evidence

ORD record
ord-573e32a42f934a1c885a00b01f45133c
Source dataset
uspto-grants-2010_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07667041B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes