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2-Acetoxy-3-dimethylamino-1,1-diphenyl-propane → 3-Dimethylamino-1,1-diphenyl-propan-2-ol

HRID 436944
Notes
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Reaction equation

HRID 436944 reaction equation
C([O:4][CH:5]([CH2:19][N:20]([CH3:22])[CH3:21])[CH:6]([C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)(=O)C>[OH-].[K+]>[CH3:22][N:20]([CH3:21])[CH2:19][CH:5]([OH:4])[CH:6]([C:13]1[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=1)[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 1

HCID 125491212-Acetoxy-3-dimethylamino-1,1-diphenyl-propane

Product 1

HCID 125491223-Dimethylamino-1,1-diphenyl-propan-2-olYield 99%

Reagents, catalysts & solvents 1

HCID 14797Potassium HydroxideSolvent

Procedure

2-Acetoxy-3-dimethylamino-1,1-diphenyl-propane (200 mg) was dissolved in methanolic potassium hydroxide (5% 10 ml.) and the solution allowed to stand overnight. Solvent was evaporated and the residue dissolved in ether and water. The ether extract was dried and evaporated to give 3-dimethylamino-1,1-diphenyl-propan-2-ol (170 mg., 97%), m.p. 72° - 73°.

Workup

  1. customSolvent was evaporated
  • dissolutionthe residue dissolved in ether
  • extractionThe ether extract
  • customwas dried
  • customevaporated
  • Sources & evidence

    ORD record
    ord-d0c44a2c9e8a4dd7b1ea2d5809cfe90d
    Source dataset
    uspto-grants-1977_06
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US04028415

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes