Hydrochloric Acid → Phenolate Sodium

HRID 1034051Notes

Reaction equation

HRID 1034051 reaction equation
[C:1]([O:8][CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)(=[O:7])[CH2:2][CH2:3][C:4]([OH:6])=[O:5].C(Cl)(=O)C([Cl:19])=O.[C:22]1([OH:28])[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1.[H-].[Na+:30].Cl>O1CCCC1.C(OCC)(=O)C>[Cl:19][C:4]([CH2:3][CH2:2][C:1]([O:8][CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)=[O:7])=[O:5].[C:22]1([O-:28])[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1.[Na+:30].[C:1]([O:8][CH2:9][C:10]1[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=1)(=[O:7])[CH2:2][CH2:3][C:4]([O:6][C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1)=[O:5]

Participants

10

Conditions

Temperature
0 °C

Procedure

Benzyl 3-chloroformylpropionate was prepared from benzyl hydrogen succinate (1.96 g) and oxalyl chloride (0.9 ml) in an usual manner. A solution of sodium phenolate, which was prepared from phenol (1.77 g) and sodium hydride (60% dispersion in mineral oil, 1.13 g) in tetrahydrofuran (20 ml), was added to a solution of the acid chloride in tetrahydrofuran (20 ml) at 0° C. After stirred at 0° C. for 30 minutes, the mixture was poured into a mixture of ethyl acetate and 1N hydrochloric acid. The organic layer was separated, washed with water, and dried over magnesium sulfate. After evaporation of the solvent, the residue was chromatographed on silica gel (50 g eluting with a mixture of ethyl acetate and hexane (1:10→1:5) to give benzyl phenyl succinate (2.15 g) as colorless crystals.

Workup

  1. customThe organic layer was separated
  2. washwashed with water
  3. dry with materialdried over magnesium sulfate
  4. customAfter evaporation of the solvent
  5. customthe residue was chromatographed on silica gel (50 g
  6. washeluting with a mixture of ethyl acetate and hexane (1:10→1:5)

Sources & evidence

ORD record
ord-e511f774d90943fc9b251aad47b79c61
Source dataset
uspto-grants-1994_05
Patent number
US05312829

Reaction notes

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