Hydrochloric Acid → 4-(benzylamino)benzoic acid

HRID 1703078Notes

Reaction equation

HRID 1703078 reaction equation
[CH2:1]([NH:8][C:9]1[CH:19]=[CH:18][C:12]([C:13]([O:15]CC)=[O:14])=[CH:11][CH:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(O)C.O.[OH-].[K+].Cl>O>[CH2:1]([NH:8][C:9]1[CH:10]=[CH:11][C:12]([C:13]([OH:15])=[O:14])=[CH:18][CH:19]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

6

Procedure

A mixture of 6.0 g. of ethyl p-benzylaminobenzoate (prepared as described in Example 9), 100 ml. of ethanol-water (9:1) and 6.0 g. of potassium hydroxide are refluxed for 3.5 hours. The mixture is acidified with concentrated hydrochloric acid, diluted with water, chilled, filtered and the solid washed with water to give pale cream crystals, m.p. 165°-168° C. Recrystallization from ethanol gives tan crystals, m.p. 167°-169° C.

Workup

  1. additionA mixture of 6.0 g
  2. temperaturechilled
  3. filtrationfiltered
  4. washthe solid washed with water
  5. customto give pale cream crystals, m.p. 165°-168° C
  6. customRecrystallization from ethanol
  7. customgives tan crystals, m.p. 167°-169° C.

Sources & evidence

ORD record
ord-767ea7d8626944c69d29f36320a822f0
Source dataset
uspto-grants-1982_09
Patent number
US04350822

Reaction notes

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