Hydrochloric Acid → HCID 12132292, compound

HRID 1824816Notes

Reaction equation

HRID 1824816 reaction equation
[CH3:1][O:2][C:3]1[CH:25]=[CH:24][CH:23]=[CH:22][C:4]=1[CH2:5][O:6][C:7]1[CH:12]=[CH:11][C:10]([C:13](=[O:21])[CH2:14][CH2:15][C:16]([O:18]CC)=[O:17])=[CH:9][CH:8]=1.[OH-].[Na+].Cl>C(O)C>[CH3:1][O:2][C:3]1[CH:25]=[CH:24][CH:23]=[CH:22][C:4]=1[CH2:5][O:6][C:7]1[CH:8]=[CH:9][C:10]([C:13](=[O:21])[CH2:14][CH2:15][C:16]([OH:18])=[O:17])=[CH:11][CH:12]=1

Participants

5

Reactant 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 21964526Ethyl 4-(4-(2-methoxybenzyloxy)phenyl)-4-oxobutyrate

Product 1

HCID 12132292HCID 12132292, compound

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

A solution of Ethyl 4-(4-(2-methoxybenzyloxy)phenyl)-4-oxobutyrate (Step B, 1.49 g, 4.3 mmol) in abs ethanol (20 ml) was treated with 1N NaOH (6 ml). The reaction mixture was stirred at room temperature for 2 hours and then acidified with 1M HCl. The resulting white solid was filtered, washed with cold water and dried under vacuum to provide the title compound.

Workup

  1. filtrationThe resulting white solid was filtered
  2. washwashed with cold water
  3. customdried under vacuum

Sources & evidence

ORD record
ord-ac294d3656104fa886761b0c0e47d0f8
Source dataset
uspto-grants-2006_05
Patent number
US07045541B2

Reaction notes

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