Ethanol → 4-(Benzyloxy)benzoic acid

HRID 1576928Notes

Reaction equation

HRID 1576928 reaction equation
N[C:2]([C:4]1[CH:17]=[CH:16][C:7]([O:8][CH2:9][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)=[CH:6][CH:5]=1)=[O:3].C([OH:20])C>[OH-].[Na+]>[C:2]([C:4]1[CH:17]=[CH:16][C:7]([O:8][CH2:9][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)=[CH:6][CH:5]=1)([OH:20])=[O:3]

Participants

4

Procedure

A mixture of 4-aminocarbonylphenoxy phenyl methane (10g) in ethanol (100ml) and sodium hydroxide (100ml., 10N) was heated under reflux with vigorous stirring for 24hrs. The reaction mixture was cooled, the precipitated sodium salt was filtered off washed with a little water then converted to 4-carboxyphenoxy phenyl methane by boiling under reflux with concentrated hydrochloric acid (100ml) for 6hr. Dilution of the cooled mixture and extraction with ether yielded 4-carboxyphenoxy phenyl methane, m.p. 188°.

Workup

  1. temperaturewas heated
  2. temperatureunder reflux
  3. temperatureThe reaction mixture was cooled
  4. filtrationthe precipitated sodium salt was filtered off
  5. washwashed with a little water
  6. temperatureunder reflux with concentrated hydrochloric acid (100ml) for 6hr
  7. extractionDilution of the cooled mixture and extraction with ether

Sources & evidence

ORD record
ord-79c4cc06627a479ca86efebca0401300
Source dataset
uspto-grants-1976_09
Patent number
US03983164

Reaction notes

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