Lithium Hydroxide → HCID 89580748, compound

HRID 1501038Notes

Reaction equation

HRID 1501038 reaction equation
[OH-].[Li+].[C:3]1([CH3:22])[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[O:9][CH:10]([C:12]1[CH:21]=[CH:20][C:15]([C:16]([O:18]C)=[O:17])=[CH:14][CH:13]=1)[CH3:11]>CO.O>[C:3]1([CH3:22])[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[O:9][CH:10]([C:12]1[CH:13]=[CH:14][C:15]([C:16]([OH:18])=[O:17])=[CH:20][CH:21]=1)[CH3:11]

Participants

5

Procedure

Lithium hydroxide (54 mg, 2.24 mmol) was added to a solution of methyl 4-(1-(o-tolyloxy)ethyl)benzoate (151 mg, 0.56 mmol) in methanol (100 mL) and water (10 mL). The reaction mixture was stirred at room temperature for 3 hours. After the reaction, the solvent was removed in vacuo. 3 mol/L aqueous hydrogen chloride was added to make pH 2˜3, and the product was extracted with dichloromethane (100 mL*3) The combined organic phase was washed with Sodium Chloride (20 mL*3), dried over anhydrous sodium sulfate, and the solvent was evaporated to dryness to give 4-(1-(o-tolyloxy)ethyl)benzoic acid (127 mg, 88%).

Workup

  1. customAfter the reaction
  2. customthe solvent was removed in vacuo
  3. addition3 mol/L aqueous hydrogen chloride was added
  4. extractionthe product was extracted with dichloromethane (100 mL*3) The combined organic phase
  5. washwas washed with Sodium Chloride (20 mL*3)
  6. dry with materialdried over anhydrous sodium sulfate
  7. customthe solvent was evaporated to dryness

Sources & evidence

ORD record
ord-b7c2b2c5845649dfa5193d1bcac7ac84
Source dataset
uspto-grants-2015_12
Patent number
US09206128B2

Reaction notes

Loading…